Clinical trials

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Condition / disease
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Status: Not yet recruiting

tDCS for Reducing the Incidence of OEI After Cesarean Section

Cesarean section is the most common obstetric surgery worldwide. Epidural anesthesia has become the preferred anesthesia method for cesarean sections due to its definite analgesic effect and minimal impact on mother and baby. To ensure postoperative analgesia, intrathecal administration of morphine (the preferred opioid for obstetric intrathecal analgesia) is a routine clinical protocol, but morphine-induced postoperative pruritus is a common adverse reaction. A study targeting the cesarean section population confirmed that the incidence of pruritus after epidural morphine administration is as high as 40%-75%.Transcranial direct current stimulation (tDCS) can enhance the activity of GABAergic inhibitory interneurons in the spinal dorsal horn through the cortical-spinal descending pathway, reverse the inhibitory effect of morphine on them, and restore negative feedback regulation of itch-specific GRPR⁺ neurons; at the same time, it downregulates the phosphorylation level and membrane expression of μ-opioid receptors in the spinal dorsal horn, weakening the receptor activation efficiency of morphine. On the other hand, tDCS can reduce peripheral nerve excitability, decrease mast cell degranulation in the skin, and reduce the release of histamine and tryptase; simultaneously, it inhibits the activation of glial cells in the spinal cord/cortex, decreases the secretion of pro-inflammatory factors such as TNF-α and IL-6, and blocks the vicious cycle of 'inflammation-receptor upregulation-itch exacerbation,' thereby reducing the occurrence of itch.This study aims to explore the effect of transcranial direct current stimulation (tDCS) on the incidence of morphine-induced itching after cesarean section by inhibiting the central itch perception circuits in cesarean section patients and antagonizing the disinhibitory effects mediated by μ-opioid receptors in the spinal dorsal horn.

Participants needed: 104
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jul 2, 2026
Eligibility criteria

Age 18-40 years, gestational age 37-41 weeks, singleton full-term pregnancy; [+4]

Presence of contraindications for tDCS (such as skull defects, intracranial meta... [+4]

Status: Not yet recruiting

RN1701 Injection in the Treatment of Relapsed/Refractory B-Cell Lymphomas

This single-arm, open-label pilot study will assess the safety and efficacy of RN1701, a bispecific CD19/CD20-targeted allogeneic CAR-T-cell product, in patients with relapsed or refractory B-cell lymphoma. Up to 19 participants will be enrolled in a conventional 3 + 3 dose-escalation scheme. The primary objective of the study is to evaluate the safety and feasibility of RN1701 for the treatment of relapsed/refractory B-cell lymphoma. The secondary objective is to evaluate the efficacy of RN1701 for the treatment of relapsed/refractory B-cell lymphoma. The exploratory objective is to evaluate the expansion, persistence, and ability of RN1701 to deplete CD19- and/or CD20-positive cells in patients with relapsed/refractory B-cell lymphoma.

Participants needed: 10
Trial details
Phase: Phase 1, Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Apr 2, 2026
Eligibility criteria

Voluntary participation; full understanding of the study and provision of writte... [+15]

Malignancy that received curative therapy and has shown no evidence of active di... [+32]

Status: Recruiting

QL1706 Plus Chemotherapy as Neoadjuvant Therapy in Triple-Negative Breast Cancer

This is a single-center, single-arm, prospective study enrolling 30 patients with stage II-III triple-negative breast cancer. The neoadjuvant regimen consists of QL1706 combined with carboplatin plus albumin-bound paclitaxel (21-day cycles for 4 cycles) followed by QL1706 combined with doxorubicin/epirubicin plus cyclophosphamide (21-day cycles for 4 cycles). The treatment observation period is 1 year, and the primary endpoint is the pathological complete response rate.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Mar 2, 2026Locations: 1
Eligibility criteria

Histologically or cytologically confirmed newly diagnosed ER-/HER2- breast cance... [+8]

History of invasive malignancies within 5 years prior to signing the informed co... [+9]

Status: Not yet recruiting

Effect of PAE Hydrogel Loaded With tRF-ASO-Exo on Patients With Diabetic Ocular Surface Diseases

The purpose of this study is to determine whether poly(β-amino ester)(PAE)hydrogel loaded with tRNA-derived fragments-antisense oligonucleotides-exosomes(tRF-ASO-Exo) could alleviate symptoms in patients with diabetic ocular surface diseases(DOSD).

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Feb 4, 2026
Eligibility criteria

1. Patients with fasting blood glucose ≥ 7.0 mmol/L or 2-hour postprandial blood...

Any past or current malignancy in or around the eye. [+18]

Status: Recruiting

Dynamic Airway Resistance & ML: Guide Sputum Suction in Ventilated Patients

Research has shown that timely suctioning not only improves survival rates but also enhances the quality of life in ventilator-dependent patients. However, clinical judgment on the optimal timing for suctioning currently relies primarily on physician experience, lacking scientific evidence \[10\]. Airway viscous resistance reflects the frictional resistance encountered by gas flow within the airways and is closely associated with airway patency. When airway secretions increase, viscous resistance undergoes dynamic changes. Therefore, analyzing these dynamic variations in viscous resistance derived from ventilator waveforms to determine the optimal suctioning timing and assess its clinical impact on the progression of pulmonary inflammation holds significant scientific value and offers new insights and methodologies for clinical practice.

Participants needed: 258
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jan 29, 2026Locations: 3
Eligibility criteria

Clinical diagnosis of Acute Respiratory Distress Syndrome (ARDS) [+2]

Clinical diagnosis of multiple organ failure; [+1]

Status: Recruiting

Clinical Study of Thiopegfilgrastim for Preventing Bone Marrow Suppression in Thoracic Tumor Chemoradiotherapy

This is a prospective observational study designed to observe and evaluate the safety and efficacy of mecapegfilgrastim in the treatment of moderate-to-severe myelosuppression associated with concurrent chemoradiotherapy. The project will provide more robust evidence-based medical support for the use of long-acting granulocyte-stimulating agents in patients undergoing concurrent chemoradiotherapy.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

Aged 18-75 years at the time of giving informed consent, both sexes eligible [+5]

Pregnant or lactating women [+3]

Status: Recruiting

Effects of taVNS Combined With Dexmedetomidine on POVN

To explore the effects and possible mechanisms of dexmedetomidine combined with taVNS on the incidence of postoperative nausea and vomiting in female patients undergoing laparoscopic surgery

Participants needed: 176
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Dec 9, 2025Locations: 1
Eligibility criteria

Women aged 18 to 65; [+4]

Patients with ASA anesthesia classification ≥ III; [+9]

Status: Recruiting

Prospective Cohort Control Study on Changes in Gut Microbiota in Ischemic Stroke

1. Stroke stands as one of the leading causes of death and long-term disability worldwide, imposing a substantial socioeconomic burden. Annual new stroke cases are estimated between 9.5 million and 10.6 million. Stroke survivors commonly face challenges of poor long-term functional outcomes and compromised immunity, which not only drive quality-of-life deterioration but also fuel the persistent escalation of socioeconomic burdens. However, current clinical treatments for stroke prognosis improvement remain limited. In recent years, with the emergence of the "microbiota-gut-brain axis" concept and advancing research, the role of gut microbiota in stroke onset, progression, and prognosis regulation has garnered increasing attention. The gut-brain axis is a complex bidirectional communication network connecting the central nervous system with the gut and its microbiota, centered on the integration of the microbiota-gut-brain axis concept. Its signaling mechanisms primarily involve multiple pathways including neural (e.g., vagus nerve), endocrine (e.g., HPA axis and gut hormones), immune (e.g., cytokines), and microbial metabolic pathways (e.g., short-chain fatty acids (SCFAs) and neuroactive substances). Dysregulation of the gut-brain axis has been proven closely associated with various diseases, including irritable bowel syndrome (IBS) characterized by visceral hypersensitivity and motility abnormalities, inflammatory bowel disease (IBD) often accompanied by emotional comorbidities, autism spectrum disorder (ASD) with gastrointestinal symptoms and behavioral core symptoms, depression and anxiety related to microbiota dysbiosis and inflammation, as well as Parkinson's disease (PD) with pathological origins potentially originating in the gut. Recent studies support that gut microbiota interact with ischemic stroke through the gut-brain axis, thereby modulating stroke pathogenesis. Gut microbiota can regulate innate and adaptive immune responses and their derived metabolites through neural pathways, influencing host brain function and behavior. Gut microbiota metabolites-short-chain fatty acids (SCFAs) such as butyrate-reduce neuroinflammation and brain injury by promoting regulatory T cell differentiation and secretion of anti-inflammatory factors IL-10 and TGF-β, suppressing pro-inflammatory Th1/Th17 responses, and enhancing expression of blood-brain barrier tight junction proteins Occludin and ZO-1. Compared to traditional stroke treatments, gut microbiota therapy breaks the time window limitation. Even days after stroke, restoring a youthful gut microbiome can reduce neuroinflammation and promote recovery in stroke patients. This effect is largely mediated by metabolites produced by bacteria, particularly short-chain fatty acids. Although existing studies have demonstrated the crucial role of gut microbiota in stroke treatment, the mechanisms underlying its effects on improving physiological and behavioral functions in stroke patients, as well as the underlying mechanisms, remain insufficiently explored. 2. Purpose of this study To investigate the mechanisms by which gut microbiota and their metabolites improve the physiological and neurological functions of stroke patients, and to provide new therapeutic approaches for improving the prognosis of stroke patients. 3. Research Design 3.1 Research Methodology This is a single-center, non-interventional, cohort-controlled clinical study that randomly enrolled 100 stroke patients and 100 healthy individuals. The participants were divided into a stroke group (case group, CS group) and a healthy control group (CON group), with 100 cases in each group. The primary objectives were to investigate the gut microbiota composition, intestinal barrier function, and inflammatory cytokine levels in stroke patients versus healthy controls, while exploring the mechanisms of beneficial gut microbiota in stroke recovery. This research may provide new therapeutic approaches to address current treatment limitations.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Dec 9, 2025Locations: 1Duration: 6 Months
Eligibility criteria

Not listed

Status: Recruiting

Clinical Study of Fospropofol Disodium for Injection in the Painless Endoscopic Diagnosis and Treatment

This is a study on the efficacy and safety of fospropofol disodium for injection in painless endoscopic diagnosis and treatment, project No.2024-YCRF-M1021, which will take more than 2 years to complete. This is a multicenter, randomized, double-blind, controlled clinical study. Using a computer-generated randomized number table, the patients were divided into two groups: the group L (fospropofol disodium group) and the group B (propofol group). After determining the group of enrolled patients, the drug was administered by two fixed anesthesiologists By participating in this study, it is possible to make your anesthesia induction stable, stable intraoperative circulation, awake and safe and comfortable, to reduce the incidence of intraoperative hypoxemia, intraoperative awareness, cardiovascular and cerebrovascular malignant events (malignant arrhythmia, cardiac arrest), which is conducive to your rapid postoperative recovery and reduce hospitalization costs.

Participants needed: 426
Trial details
Age: 50-65Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Sep 30, 2025Locations: 5
Eligibility criteria

Age 50-65 years, weight 40-65kg, male or female; [+3]

Patients with simple and painless gastroscopy [+6]

Status: Recruiting

Clinical Application Research of 5-Degree (0.05 D) Precision Optometry in Corneal Refractive Surgery

In recent years, the incidence of myopia has been high globally and is exhibiting a rapid upward trend, with projections estimating it will reach 49.8% by 2050. Corneal refractive surgery has become a primary method for correcting myopia, demonstrating significant efficacy and favorable safety. However, studies indicate that overcorrection or undercorrection can occur following refractive surgery. Reports have shown that three months post-SMILE surgery, 20% of eyes had residual refractive errors ≥ 0.50 D, and 6% had errors ≥ 1.00 D. We hypothesize that this may be related to imprecise preoperative refraction, subsequently affecting postoperative visual quality. Due to limitations in lens manufacturing precision, the widely used increment for sphere correction remains 0.25 D. However, this may prevent some patients from achieving their optimal corrected state. Studies have reported that 95% of individuals are sensitive to diopter changes below 0.25 D, and 44% can distinguish changes smaller than 0.125 D. Other research suggests that adjusting spherical power in 0.05 D increments yields better corrected visual acuity. Furthermore, scholars have reported that 0.05 D precision refraction can significantly improve the red-green balance test rate, enabling myopic patients to achieve better visual quality. Therefore, improving refraction precision could provide patients with superior visual outcomes. Currently, the Binocular Wavefront Optometry Machine (BWFOM, Ai-Zhitong Medical Technology Co., Ltd., Zhejiang, China) can perform objective and subjective refraction with 0.05 D increments for both sphere and cylinder correction, while also separately measuring higher-order aberrations (HOAs) and lower-order aberrations (LOAs). Given the scarcity of research on the outcomes of 0.05 D refraction for SMILE and FS-LASIK procedures, this study aims to evaluate visual acuity, aberrations, and refractive status in patients following SMILE and FS-LASIK surgery. The primary objective is to investigate whether preoperative 0.05 D precision refraction using the BWFOM can enhance postoperative visual quality for SMILE and FS-LASIK patients.

Participants needed: 600
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Aug 28, 2025Locations: 1
Eligibility criteria

The diopter is relatively stable (the diopter increases within -0.50D per year f... [+4]

Patients with history of eye surgery and trauma; [+5]

Status: Recruiting

Study of Sivelestat Sodium in OPCABG

The goal of this clinical trial is to learn if drug Sivelestat Sodium works to improve the prognosis of off-pump coronary artery bypass grafting (OPCABG) in adults. It will also learn about the safety of drug Sivelestat Sodium. The main questions it aims to answer are: * Does drug Sivelestat Sodium have a protective effect on myocardial injury after OPCABG? * Does Sivelestat Sodium exert a protective effect on myocardial inflammatory stress after OPCABG? Researchers will compare drug Sivelestat Sodium to a placebo (a look-alike substance that contains no drug) to see if drug Sivelestat Sodium works to protect myocardium following OPCABG. Participants will: * Accept drug Sivelestat Sodium injection or a placebo 2 h after OPCABG for 72 h. * Undergo a series of blood tests and echocardiography examinations after the OPCABG.

Participants needed: 62
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Aug 12, 2025Locations: 1
Eligibility criteria

Undergoing elective OPCABG (≥2 bridged vessels). LVEF≥35%, no severe liver or ki...

Emergency operation, combined valve surgery or aortic surgery. Usage of immunosu... [+3]

Status: Not yet recruiting

Effect of Digital Intervention on Self-management of Hypertensive Patients at High Risk of Stroke

Stroke is the second leading cause of death in the world, and the number of stroke patients in China ranks the first in the world. Hypertension is the most important risk factor. Studies have shown that 80% of stroke can be prevented by controlling risk factors. However, the management level of hypertension patients in China is still low, and their self-management ability is insufficient. Digital health management, such as remote monitoring, AI and mobile health platforms, provides a new way for hypertension prevention and control. Foreign studies have shown that digital interventions can effectively improve patients' self-management behaviors, such as diet, exercise and blood pressure control. Interventions based on wechat, APP and other tools in China have also achieved positive results, but face challenges such as patient acceptance, system adaptation and data continuity. Based on behavior change wheel (BCW) theory \*\* and digital platform, this study formulated personalized intervention programs for hypertension patients in high-risk groups of stroke, and promoted health behavior change from three aspects of \*\* ability, motivation and opportunity \*\*. By improving disease cognition and strengthening self-management, the incidence of stroke can be ultimately reduced, and a new strategy for hypertension prevention and control in the community can be provided.

Participants needed: 120
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jul 28, 2025
Eligibility criteria

Not listed

Status: Recruiting

Clinical Study of SMILE 4.0-VISULYZE in Correcting Refractive Errors

The aim of this study is to further optimize the surgical input parameters for patients undergoing Small Incision Lenticule Extraction (SMILE) using the regression model established by the SMILE 4.0-VISULYZE system, thereby achieving satisfactory postoperative refractive outcomes. In this study, patients scheduled for SMILE surgery at the investigators' hospital will be divided into two groups: a conventional group, where the input parameters are adjusted based on historical experience according to the patient's refractive error, and a 4.0-VISULYZE group, where the input parameters are optimized using the SMILE 4.0-VISULYZE system. The investigators will compare the postoperative outcomes between the two groups, including uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), spherical power, cylindrical power, spherical equivalent (SE), and the proportions of patients achieving postoperative visual acuity ≥0.8, ≥1.0, and ≥1.2 at 1 day, 10 days, 1 month, 3 months, 6 months, and 1 year post-surgery. Additionally, the investigators will evaluate the proportions of patients with postoperative SE within ±0.50D and ±1.0D, as well as postoperative cylindrical power within ±0.50D and ±1.0D, to assess the efficacy and safety of the SMILE 4.0-VISULYZE system in treating refractive errors.

Participants needed: 600
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: May 28, 2025Locations: 2
Eligibility criteria

The diopter is relatively stable (the diopter increases within -0.50D per year f... [+4]

Patients with history of eye surgery and trauma; [+5]

Status: Not yet recruiting

Autologous Bone Marrow Mesenchymal Stem Cell Therapy for Ischemic Stroke

Stroke is a group of diseases mainly characterized by cerebral ischemia or hemorrhage, with a high fatality rate and disability rate. It has now become a major obstacle to social and economic development. Stem cells are a type of primitive cells with self-renewal, proliferation and differentiation potential. Under certain conditions, they can differentiate into cells of various tissues and organs. They have now become one of the key research directions for the repair of functional disorders after ischemic stroke. Compared with other types of stem cells, bone marrow mesenchymal stem cells (BMSCs) have the advantages of being relatively easy to obtain with less tissue damage, convenient and rapid in vitro expansion and culture, and the ability to actively migrate to the lesion area after injection without the risk of canceration. This study plans to recruit and screen 12 subjects with ischemic stroke, divided into three groups (Ommaya drug reservoir group, low-dose internal carotid artery transplantation group, and high-dose internal carotid artery transplantation group), with 4 subjects in each group, for a clinical study of ABMSCs treatment for functional disorders after ischemic stroke. In accordance with the established treatment protocol, bone marrow will be collected from subjects during the stable phase of their condition, and ABMSCs will be infused three times via Ommaya drug reservoir/internal carotid artery within 1-6 months after collection. The study will assess the improvement of motor function in patients and analyze the feasibility and effectiveness of this therapy, laying a solid foundation for future clinical applications.

Participants needed: 12
Trial details
Phase: Phase 1, Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: May 31, 2025Locations: 1
Eligibility criteria

Age 18-65 years, both male and female [+5]

Patients with needle phobia or lumbar spine disease affecting bone marrow aspira... [+16]

Status: Recruiting

Study on the Molecular Mechanism of Berberine to Improve Type 2 Diabetes Mellitus Complicated With Depression

The incidence of type 2 diabetes with comorbid depression (T2DD) is notably high, characterized by prolonged disease duration and susceptibility to recurrence. The preliminary experiments identified 5-AVAB, a gut microbiota-derived metabolite, as a potential novel biomarker for T2DD progression. Given the absence of existing research in this area, it warrants in-depth investigation. The investigators plan to collect fecal and serum samples from participants with type 2 diabetes and those with T2DD to quantify 5-AVAB levels, as well as conduct in vitro gut microbiota culturing and sequencing studies.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Affiliated Hospital of Nantong UniversityUpdated: May 28, 2025Locations: 1Duration: 3 Years
Eligibility criteria

Aged 18-65 years (including the critical value), regardless of gender; [+3]

Those who do not meet the inclusion criteria; [+8]

Status: Recruiting

The Safety and Efficacy of Radiofrequency Ablation After Left Atrial Appendage Occlusion.

Objective: To evaluate the safety and efficacy of transcatheter atrial fibrillation ablation 1 month after WATCHMAN FLX left atrial appendage closure in patients with nonvalvular atrial fibrillation.

Participants needed: 210
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Affiliated Hospital of Nantong UniversityUpdated: May 22, 2025Locations: 1
Eligibility criteria

≥18 years of age, diagnosed with nonvalvular atrial fibrillation; [+3]

valvular heart disease or other structural heart disease that causes atrial fibr... [+5]

Status: Recruiting

A Clinical Study on the Efficacy and Safety of Zonisamide as a First Add-On Treatment in Epileptic Seizures

This study primarily aims to assess the efficacy and safety of zonisamide when used as an adjunctive therapy for focal epilepsy. The main questions it aims to answer are: 1. Does the frequency of epileptic seizures decrease after oral zonisamide, and does it improve cognitive function? 2. Are there any treatment-emergent adverse events associated with oral administration of zonisamide?

Participants needed: 30
Trial details
Phase: Phase 4Age: 1-14Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: May 13, 2025Locations: 1
Eligibility criteria

Consent to participate in the clinical trial, and the trial subject and/or legal... [+4]

History of zonisamide treatment. [+9]

Status: Recruiting

Wearable Devices Empowering Active Health Initiatives for High-Risk Stroke Populations

The purpose of this study is to evaluate the control effect of smart wearable devices on key risk factors in the high-risk populations for stroke

Participants needed: 300
Trial details
Age: 30+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Apr 30, 2025Locations: 1
Eligibility criteria

Diagnosed with hypertension; [+6]

Diagnosed with malignancies; [+3]

Status: Not yet recruiting

Clinical Study on the Efficacy and Safety of Hydromorphone for ICU Analgesia

This study is a prospective, single-center clinical study to evaluate the advantages, extensibility and safety of hydromorphone as an analgesic drug in ICU, and to compare it with remifentanil, a traditional sedative drug. These conclusions can guide us to understand the characteristics of analgesic drugs, carry out appropriate pain management, improve the status of ICU patients, and improve the quality of life of patients.

Participants needed: 300
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Mar 14, 2025Locations: 1
Eligibility criteria

Age ≥18 years and ≤75 years; [+2]

Under 18 years of age, or over 75 years of age; [+18]

Status: Recruiting

Pretreatment With HCQ Before Radiotherapy and Chemotherapy in Advanced NPC Patients

Dormant cancer cells that survive anti-cancer therapy can lead to cancer recurrence and disseminated metastases that prove fatal in most cases. Recently, specific dormant polyploid giant cancer cells (PGCC) have drawn the investigators' attention because of their association with the clinical risk of nasopharyngeal carcinoma (NPC) recurrence, as demonstrated by previous clinical data. In study, the investigators report the biological properties of PGCC, and reveal that autophagy is a critical mechanism of PGCC induction. Moreover, pharmacological inhibition of autophagy greatly impaired PGCC formation, significantly suppressing metastasis and improving survival in a mouse model. Mechanistically, chemotherapeutic drugs partly damaged mitochondria, and activated autophagy to promote PGCC formation. High numbers of PGCCs correlated with shorter recurrence time and worse survival outcomes in NPC patients. Collectively, these findings suggest a therapeutic approach of targeting dormant PGCCs in cancer. Pretreatment with an autophagy inhibitor (HCQ) before chemotherapy and radiotherapy could prevent formation of therapy-induced dormant polyploid giant cancer cells, thereby reducing recurrence and metastasis of nasopharyngeal carcinoma.

Participants needed: 30
Trial details
Age: 20-70Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Feb 18, 2025Locations: 1
Eligibility criteria

Clinical diagnosis of NPC. [+2]

With metastasis before the first treatment.

Status: Recruiting

Polatuzumab, Rituximab and Orelabrutinib Combination Regimen (PRO) in the Treatment of Elderly Frail Patients with Treatment-naive Non-GCB DLBCL

This prospective, single-arm, multicenter clinical study aims to enroll 30 frail elderly patients with Non-GCB DLBCL. This study is to evaluate the preliminary efficacy and safety of the combination of Polatuzumab, Rituximab, and orelabrutinib in this population. The primary endpoint is CR rate after induction therapy.

Participants needed: 30
Trial details
Phase: Phase 2Age: 60+Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Feb 4, 2025Locations: 2
Eligibility criteria

Patients with histopathologically confirmed DLBCL; [+4]

Accompanied by uncontrolled cardiovascular and cerebrovascular diseases, Coagulo... [+3]

Status: Recruiting

Laparoscopic Surgical Systems for Gynecological and Remote Surgical Treatment.

Remote robot-assisted laparoscopic surgery will be performed for gynecological surgical treatment through 5G network, while the safety and effectiveness will be studied.

Participants needed: 5
Trial details
Age: 18-80Biological sex: FemaleType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jan 28, 2025Locations: 1
Eligibility criteria

Patients who require endoscopic surgery [+1]

Patients with malignant tumors with clinical stage IV [+6]

Status: Recruiting

Evaluation of Irinotecan Liposome (II) Combined With 5-FU, LV, and Bevacizumab for mCRC

To observe and evaluate the efficacy and safety of irinotecan liposome (II) combined with 5-fluorouracil(5-FU), calcium leucovorin(LV), and bevacizumab in the treatment of metastatic colorectal cancer.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jan 28, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years old and ≤ 75 years old, gender is not limited; [+9]

Have had a malignant tumor other than colorectal cancer within 5 years before th... [+12]

Status: Not yet recruiting

The Impact of Smoking on the Prognosis of Elderly Surgical Patients

Postoperative delirium is a common complication that frequently occurs in elderly patients after surgery. It not only increases the length of hospital stays and healthcare costs but also raises the incidence of postoperative cognitive dysfunction and even mortality. However, the underlying mechanisms of its onset are not yet fully understood. Evidence suggests that smoking can lead to gut microbiota dysbiosis and metabolic dysfunction, and the gut microbiota and its metabolites play a crucial role in cognitive function through the gut-brain axis. Yet, no studies have reported whether smoking could affect the occurrence of postoperative delirium and the quality of postoperative recovery through the gut microbiota. This study aims to observe the incidence of postoperative delirium and the postoperative recovery quality scores between smokers and non-smokers.

Participants needed: 121
Trial details
Age: 60-80Biological sex: AllType: ObservationalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jan 16, 2025Locations: 1
Eligibility criteria

Age >60 years; [+3]

Mini-Mental State Examination (MMSE) score <23; [+5]

Status: Recruiting

A Study of CAR T-Cells in Relapsed/Refractory Hematologic Malignancy

This study is a single-center, open-label clinical trial of single-dose of CAR T-cells in subjects with relapsed/refractory hematologic malignancy.

Participants needed: 9
Trial details
Phase: Early Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: Affiliated Hospital of Nantong UniversityUpdated: Jan 3, 2025Locations: 1
Eligibility criteria

Voluntarily participate in the clinical study. The individual or the legal guard... [+32]

CNS-3 disease is defined as detectable tumor cells in the cerebrospinal fluid (C... [+33]