Clinical trials

25

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Condition / disease
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Status: Not yet recruiting

Effect of LSD on Renal Function in Cirrhosis Patients With Portal Hypertension Bleeding (2-Year Follow-Up)

Patients with liver cirrhosis often have impaired or at-risk kidney function due to the close link between liver and kidney (hepatorenal syndrome). Laparoscopic Splenectomy and Azygoportal Disconnection (LSD) is commonly used to treat Cirrhosis with Portal Hypertension Bleeding in these patients, but its impact on kidney function over 2 years is unclear. This study will follow patients undergoing laparoscopic splenectomy to measure changes in kidney function before and after surgery, identify risk factors for kidney damage and whether LSD can improve kidney function in the long term, and help improve care to protect kidney function in cirrhotic patients .

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Northern Jiangsu People's HospitalUpdated: May 18, 2026Duration: 2 Years
Eligibility criteria

Confirmed diagnosis of liver cirrhosis (clinical, laboratory, imaging) [+7]

Child-Pugh Class C liver cirrhosis [+6]

Status: Not yet recruiting

Effect of Laparoscopic Splenectomy on Renal Function in Cirrhotic Patients With Hypersplenism (2-Year Follow-Up)

Patients with liver cirrhosis often have impaired or at-risk kidney function due to the close link between liver and kidney (hepatorenal syndrome). Laparoscopic splenectomy is commonly used to treat splenomegaly and hypersplenism in these patients, but its impact on kidney function over 2 years is unclear. This study will follow patients undergoing laparoscopic splenectomy to measure changes in kidney function before and after surgery, identify risk factors for kidney damage and whether laparoscopic splenectomy can improve kidney function in the long term, and help improve care to protect kidney function in cirrhotic patients .

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Northern Jiangsu People's HospitalUpdated: May 18, 2026Locations: 1Duration: 2 Years
Eligibility criteria

Confirmed diagnosis of liver cirrhosis (clinical, laboratory, imaging) [+7]

Child-Pugh Class C liver cirrhosis [+6]

Status: Not yet recruiting

Long-term Efficacy and Safety of LSD Versus TIPS for Cirrhotic Portal Hypertension Bleeding and Hypersplenism

This study aims to compare two treatments for cirrhotic portal hypertension with acute esophagogastric variceal bleeding and hypersplenism: laparoscopic splenectomy and azygoportal disconnection (LSD) and transjugular intrahepatic portosystemic shunt (TIPS). It is a single-center, prospective trial. The primary outcome is the incidence of post-procedure hepatic encephalopathy. Secondary outcomes include changes in hepatic venous pressure gradient, portal and hepatic artery hemodynamics, liver function, renal function, complete blood count, immune function, hepatic reserve capacity, serological markers of liver fibrosis, re-bleeding rate, hepatocellular carcinoma incidence, recompensation incidence, overall survival, and bleeding-free survival. The study will provide high-level evidence for optimal treatment selection in this patient population.

Participants needed: 140
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Northern Jiangsu People's HospitalUpdated: May 18, 2026Locations: 1
Eligibility criteria

Confirmed diagnosis of cirrhotic portal hypertension. [+5]

Liver function Child-Pugh class C (score ≥10), or Model for End-Stage Liver Dise... [+10]

Status: Not yet recruiting

Effect of Laparoscopic Splenectomy on Lipid Profiles in Cirrhotic Patients With Hypersplenism (2-Year Follow-Up)

Patients with liver cirrhosis frequently exhibit dyslipidemia due to impaired hepatic lipid synthesis, altered bile acid metabolism, and portal hypertension. Laparoscopic splenectomy is commonly used to treat splenomegaly and hypersplenism in these patients, but its impact on lipid profiles over 2 years remains poorly characterized. This study will follow patients undergoing laparoscopic splenectomy to measure changes in serum lipid parameters before and after surgery, identify risk factors for lipid profile deterioration or improvement, and determine whether laparoscopic splenectomy can ameliorate dyslipidemia in the long term, thereby informing metabolic management strategies in cirrhotic patients.

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Northern Jiangsu People's HospitalUpdated: May 14, 2026Locations: 1Duration: 2 Years
Eligibility criteria

Age 18-80 years, male or female [+5]

Child-Pugh Class C liver cirrhosis [+8]

Status: Not yet recruiting

Effect of LSD on Lipid Profiles in Cirrhosis Patients With Portal Hypertension Bleeding (2-Year Follow-Up)

Patients with liver cirrhosis frequently exhibit dyslipidemia due to impaired hepatic lipid synthesis, altered bile acid metabolism, and portal hypertension. Laparoscopic Splenectomy and Azygoportal Disconnection (LSD) is commonly used to treat Cirrhosis with Portal Hypertension Bleeding in these patients, but its impact on lipid profiles over 2 years remains poorly characterized. This study will follow patients undergoing LSD to measure changes in serum lipid parameters before and after surgery, identify risk factors for lipid profile deterioration or improvement, and determine whether LSD can ameliorate dyslipidemia in the long term, thereby informing metabolic management strategies in cirrhotic patients.

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Northern Jiangsu People's HospitalUpdated: May 14, 2026Locations: 1Duration: 2 Years
Eligibility criteria

Age 18-80 years, male or female [+6]

Child-Pugh Class C liver cirrhosis [+7]

Status: Recruiting

Vagus Nerve-guided Laparoscopic Splenectomy and Azygoportal Disconnection

This study aimed to evaluate the effectiveness and safety of vagus nerve-guided laparoscopic splenectomy and azygoportal disconnection, and to assess its impact on postoperative digestive complications and quality of life.

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Apr 1, 2026Locations: 2
Eligibility criteria

A clinical, radiological or histologic diagnosis of cirrhosis of any etiology [+4]

Delayed gastric emptying [+10]

Status: Recruiting

Efficacy of Apixaban in the Treatment of Portal Vein Thrombosis Occurring More Than One Year After LS

The purpose of this study is to determine whether Apixaban is effective and safe in the treatment of portal vein thrombosis Occurring more than one year after laparoscopic splenectomy.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

A clinical, radiological, or histologic diagnosis of cirrhosis of any etiology. [+9]

Hepatocellular carcinoma or any other malignancy. [+9]

Status: Recruiting

Efficacy of Apixaban in Treating Portal Vein Thrombosis Occurring More Than One Year After LSD

The purpose of this study is to determine whether Apixaban is effective and safe in the treatment of portal vein thrombosis Occurring more than one year after laparoscopic splenectomy and azygoportal disconnection.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

A clinical, radiological, or histologic diagnosis of cirrhosis of any etiology. [+10]

Hepatocellular carcinoma or any other malignancy. [+8]

Status: Recruiting

Hydrocortisone and Fludrocortisone for the Treatment of Septic Shock

The purpose of this study is to evaluate the efficacy and safety of the combination therapy of hydrocortisone and fludrocortisone among adult patients with septic shock.

Participants needed: 336
Trial details
Phase: Phase 4Age: 18-90Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Systemic corticosteroid therapy within the last 3 months before septic shock; [+8]

Status: Recruiting

Correlation Between Advanced Glycation End Products and Gastric Motility Disorder in Diabetes Gastroparesis

This study is a prospective observational study. The study will explore the correlation between advanced glycation end products and gastric motility disorder in diabetic gastroparesis(DGP) through the collection of blood and gastric tissue samples and relevant data of patients with DGP and control group patients without diabetes history and gastroparesis symptoms.

Participants needed: 50
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Northern Jiangsu People's HospitalUpdated: Feb 17, 2026Locations: 1Duration: 2 Weeks
Eligibility criteria

Meet the diagnostic criteria for diabetes [+7]

Currently taking prokinetic drugs, anticholinergic drugs, and dopamine drugs tha... [+4]

Status: Not yet recruiting

The Efficacy of Personalized Local Anesthetic Dosing Based on Ultrasound-Measured Nerve Cross-Sectional Area in Brachial Plexus Block: a Non-Inferiority Randomized Controlled Trial.

This is a prospective, randomized, assessor-blinded, three-arm, non-inferiority clinical trial. The study aims to compare the effectiveness and safety of an individualized dosing strategy for local anesthetic in brachial plexus blocks against two standard methods. The experimental intervention uses ultrasound to measure the cross-sectional area (CSA) of the brachial plexus nerves to calculate a patient-specific dose of 0.5% ropivacaine. This is compared to a standard weight-based dosing regimen (2.5 mg/kg) and dosing based on the anesthesiologist's clinical experience. A total of 350 adult patients scheduled for elective unilateral upper limb surgery will be randomly assigned to one of the three groups. The primary outcome is the success rate of the nerve block 30 minutes after administration. Secondary outcomes include assessments of diaphragmatic function, postoperative pain scores, the incidence of complications (such as nerve involvement or systemic toxicity), and patient satisfaction. The hypothesis is that the CSA-based dosing method will be non-inferior to the conventional methods in achieving successful anesthesia while potentially optimizing drug dosage.

Participants needed: 300
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jan 20, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Tislelizumab Combined With Thoracic Radiotherapy as Neoadjuvant Therapy for Resectable NSCLC

This study aims to explore the efficacy and safety of radiotherapy combined with immunotherapy in the neoadjuvant treatment of resectable NSCLC.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jan 9, 2026Locations: 1
Eligibility criteria

Fully understand the study and voluntarily sign the informed consent form (ICF); [+10]

Presence of locally advanced unresectable or metastatic disease; [+11]

Status: Recruiting

Efcacy and Safety of Postoperative Adjuvant Hepatic Arterial Infusion Chemotherapy With mFOLFOX in Hepatocellular Carcinoma With High-risk Recurrence Factors

This is a single-center, single-arm, prospective trial to explore the efficacy and safety of postoperative adjuvant hepatic arterial infusion chemotherapy(HAIC) with mFOLFOX in hepatocellular carcinoma with high-risk recurrence factors.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jan 13, 2026Locations: 1
Eligibility criteria

Age ≥18 years and ≤75 years. [+9]

Presence of extrahepatic metastasis, residual lesions, or recurrence on imaging... [+16]

Status: Recruiting

Efficacy and Safety of Icaritin Combined With mFOLFOX in Postoperative HCC With High-risk Recurrence Factors

This is a single-center, single-arm, prospective trial to explore the efficacy and safety of Icaritin Soft Capsules combined with postoperative adjuvant hepatic arterial infusion chemotherapy(HAIC) with Modified Folinic acid, Fluorouracil, and Oxaliplatin (mFOLFOX) in hepatocellular carcinoma (HCC) with high-risk recurrence factors.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jan 13, 2026Locations: 1
Eligibility criteria

Age ≥18 years and ≤75 years. [+9]

Presence of extrahepatic metastasis, residual lesions, or recurrence on imaging... [+16]

Status: Recruiting

Laparoscopic Partial Splenectomy for Hypersplenism in Liver Cirrhosis Patients

In this study,the researchers compared the changes in immune function-related indicators in patients with liver cirrhosis following laparoscopic partial splenectomy,to determine whether this surgical intervention can enhance postoperative immune function and thereby improve patient outcomes.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Oct 3, 2025Locations: 1
Eligibility criteria

A clinical, radiological or histologic diagnosis of cirrhosis of any etiology [+3]

Hepatocellular carcinoma or any other malignancy, [+6]

Status: Recruiting

CT-guided Localization for Micro Hepatocellular Carcinoma Before Surgical Resection

In this project, the preoperative anatomical location of micro hepatocellular carcinoma under the guidance of CT can provide guidance for accurate surgical resection. It may also shorten the operation time and reduce intraoperative bleeding.

Participants needed: 5
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

Be at least 18 years old and give informed consent to participate in the study [+4]

Child-Pugh grade C [+3]

Status: Recruiting

Effect of Thread Embedding Acupuncture on Postoperative Ileus Recovery After Colorectal Cancer Surgery: A Multicenter Randomized Controlled Trial

This multicenter, randomized, controlled trial aims to evaluate the efficacy and safety of thread embedding acupuncture (TEA) in promoting gastrointestinal recovery after laparoscopic colorectal cancer surgery. The primary outcome is the time to first flatus. Secondary outcomes include time to first defecation, tolerance to oral intake, length of hospital stay, and patient-reported quality of life.

Participants needed: 300
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Clinical Study on Laparoscopic Resection of Splenic Artery Aneurysm With Preservation of Spleen

In this study, researchers examined the changes in related indicators such as immune function, splenic vein,proper hepatic artery, and portal venous hemodynamics following laparoscopic resection of a splenic artery aneurysm. We determined the changes in these patient-related indicators after surgical treatment and whether these changes could improve patient outcomes.

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jul 8, 2025Locations: 1
Eligibility criteria

Asymptomatic splenic artery aneurysms with a diameter>2 cm,ruptured splenic arte...

Patients with malignancies Hepatic cirrhosis with portal hypertension peptic ulc...

Status: Recruiting

The Effect of Laparoscopic Splenectomy and Azygoportal Disconnection on the Immune Function for Cirrhosis Patients

In this study, the investigators compared the improvement of immune function related indicators in patients with liver cirrhosis after laparoscopic splenectomy and azygoportal disconnection. To determine whether surgical treatment can help enhance postoperative immune function and improve patient prognosis.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: May 28, 2025Locations: 1
Eligibility criteria

A clinical, radiological or histologic diagnosis of cirrhosis of any etiology [+3]

Hepatocellular carcinoma or any other malignancy, [+6]

Status: Recruiting

The Effect of Laparoscopic Splenectomy and Azygoportal Disconnection on Liver Reserve Function for Cirrhosis Patients

In this study, the investigators compared the improvement of liver reserve function related indicators in patients with liver cirrhosis after laparoscopic splenectomy and azygoportal disconnection. To determine whether surgical treatment can help enhance postoperative liver reserve function and improve patient prognosis.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: May 30, 2025Locations: 1
Eligibility criteria

A clinical, radiological or histologic diagnosis of cirrhosis of any etiology [+3]

Hepatocellular carcinoma or any other malignancy, [+6]

Status: Recruiting

The Effect of Laparoscopic Splenectomy on Liver Reserve Function for Cirrhosis Patients

In this study, the investigators compared the improvement of liver reserve function related indicators in patients with liver cirrhosis after laparoscopic splenectomy. To determine whether surgical treatment can help enhance postoperative liver reserve function and improve patient prognosis.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: May 30, 2025Locations: 1
Eligibility criteria

A clinical, radiological or histologic diagnosis of cirrhosis of any etiology [+2]

Hepatocellular carcinoma or any other malignancy, [+7]

Status: Not yet recruiting

A Study of QL1706 Combined with Nine HPV Vaccine As First-line Treatment for Persistent, Recurrent or Metastatic Cervical Cancer

The study medications were used as follows: 1 cycle every 21 days (3 weeks) of the following regimen. Test drug: QL1706, HPV 9-valent vaccine QL1706: Dose: 5 mg/kg ; intravenous infusion (ivgtt), administered on Day 1 of each cycle and every 3 weeks (21 days). Treatment will continue until loss of clinical benefit, occurrence of intolerable toxicity, patient or physician decision to discontinue treatment, death of the patient receiving the experimental treatment, or completion of 2 years of dosing (35 dosing cycles), withdrawal of informed consent by the subject, pregnancy of the subject, noncompliance with protocol or procedural requirements, or for administrative reasons. HPV 9-valent vaccine: 1st dose 1 day prior to first QL1706 administration; 2nd dose 2 months after 1st dose; 3rd dose 6 months after 1st dose.

Participants needed: 35
Trial details
Phase: Phase 2Biological sex: FemaleType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 28, 2025
Eligibility criteria

Patients with unsystematically treated cervical cancer, who voluntarily particip... [+8]

Status: Not yet recruiting

An Exploratory Clinical Study on Neoadjuvant Treatment of Hepatocellular Carcinoma with QL1706 Combined with Lenvatinib

This is a single-center, single-arm, prospective trial to explore the efficacy and safety of neoadjuvant treatment with Iparomlimab and Tuvonralimab Injection combined with lenvatinib in patients with advanced HCC

Participants needed: 30
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Mar 19, 2025
Eligibility criteria

Age ≥18 years and ≤ 75 years; [+10]

Pregnant or lactating women; [+15]

Status: Recruiting

A Pilot Study of the Effect of the Combination of Inhaled Nitric Oxide and Prone Position Under EIT Monitoring on Efficacy in Patients with ARDS

Investigating the Impact of Combined Inhaled Nitric Oxide and Prone Positioning on the Efficacy in ARDS Patients

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Jan 10, 2025Locations: 1
Eligibility criteria

Age 18-80 years; [+1]

Patients with severe asthma or acute exacerbation of chronic obstructive pulmona... [+7]

Status: Recruiting

Preliminary Efficacy Analysis of 'λ+α' Double-Tract Reconstruction After Laparoscopic Proximal Gastrectomy

The incidence of proximal gastric cancer has increased significantly in recent years. This may be due to weight gain, alcohol consumption, gastroesophageal reflux disease (GERD), and precancerous lesions. With a deeper understanding of the pattern of lymph node metastasis and the emergence of anti-reflux procedures, proximal gastrectomy has gradually received clinical attention. For early-stage upper gastric cancer and esophagogastric combination cancer cases that are expected to have a good prognosis, the ideal surgical procedure should be to preserve the distal stomach to improve the quality of life and to choose a reasonable digestive tract reconstruction method to prevent reflux. The anti-reflux effect of various proximal gastrectomy digestive tract reconstruction methods and the advantages and disadvantages of various surgical procedures are controversial, and the recognized ideal reconstruction method has not yet been established. Therefore, based on the stomach's anatomical features and the intercalated jejunum's anti-reflux mechanism, we propose a true dual-channel anastomosis for GI reconstruction, i.e., the "λ+α dual-channel anastomosis". This study aimed to investigate the efficacy and safety of proximal gastrectomy combined with "λ+α double-channel anastomosis" in the treatment of early gastric cancer.

Participants needed: 60
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Northern Jiangsu People's HospitalUpdated: Aug 15, 2024Locations: 1
Eligibility criteria

Not listed