Clinical trials

10

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
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Status: Not yet recruiting

Clinical Study on the Efficacy and Safety of CAR-DC in the Treatment of Advanced Solid Tumors

This is a prospective, open label, single arm clinical trial to evaluate the safety and the preliminary efficacy of chimeric antigen receptor-dendritic cell (CAR-DC) in the treatment of advanced solid tumors positive for one of the following antigens: ephrin type-A receptor 2 (EphA2), claudin-18 isoform 2 (CLDN18.2) , trophoblast cell surface antigen 2 (Trop2), human epidermal growth factor receptor 2 (HER2), guanylyl cyclase-C (GCC), glypican-3 (GPC3) and carcinoembryonic antigen (CEA).

Participants needed: 10
Trial details
Phase: Early Phase 1Age: 18-70Biological sex: AllType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Aged 18-70, regardless of gender; [+11]

Pregnant and lactating women; (The pregnancy test results are included in the CR... [+8]

Status: Recruiting

Iruplinalkib in ALK-Positive Advanced Lung Adenocarcinoma After Lorlatinib

This observational study aims to evaluate the real-world effectiveness and safety of iruplinalkib in patients with advanced ALK-positive lung adenocarcinoma who have progressed on or are intolerant to prior lorlatinib therapy. The results are expected to provide real-world evidence to inform clinical decision-making for this heavily pretreated patient population.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Peking University Shenzhen HospitalUpdated: Jan 29, 2026Locations: 1
Eligibility criteria

Population: Male or female patients aged ≥18 years. [+6]

Lack of Exposure: Patients who never actually received iruplinalkib or took only... [+4]

Status: Recruiting

The Effective Blood Concentration of Ciprofol

1. Eligible patients were selected and enrolled in the study. 2. General anesthesia was induced using ciprofol in all participants, with standardized evaluation of consciousness levels during induction. 3. The patients' pain and cognition are followed up after surgery.

Participants needed: 101
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Peking University Shenzhen HospitalUpdated: Jan 6, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Patients aged 18-65 years [+3]

Recent use of sedatives or opioid analgesics [+5]

Status: Recruiting

Effect of MGRNOX-Guided General Anesthesia on Opioid Consumption in Patients

1. Pain management is a crucial part of general anesthesia surgery. Nociception monitoring can help anesthesiologists better titrate the use of intraoperative analgesic drugs, especially the opioid. 2. Although a variety of nociception monitoring devices have been developed to date, there is not a specific monitoring indicator that serves as the "gold standard" to objectively guide analgesic management in general anesthesia. 3. The MGRNOX index, which is derived from electroencephalogram (EEG), is used to reflect the correlation between noxious stimuli and opioid analgesics in a state of general anesthesia by converting and quantifying the EEG signals collected by the instrument. However, no studies have so far verified the effect of the MGRNOX index-guided analgesic management of general anesthesia on the consumption of opioids in patients. 4. This study aims to explore the effect of MGRNOX index-guided general anesthesia on opioid consumption in patients undergoing laparoscopic cholecystectomy and the primary hypothesis of our study is that using the MGRNOX index to guide intraoperative pain management during general anesthesia can significantly reduce the consumption of remifentanil during the surgery.

Participants needed: 112
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Dec 18, 2025Locations: 1
Eligibility criteria

Age ≥18 years old and < 65 years old; [+2]

Pregnancy or lactation period; [+10]

Status: Recruiting

Effects of Esketamine Combined With Dexmedetomidine on Postoperative Sleep Quality

1. Eligible patients are randomly divided into experimental and control groups; 2. The experimental group is given esketamine combined with dexmedetomidine,while the control group is given normal saline; 3. The patients' sleep, pain, and cognition are followed up after surgery.

Participants needed: 96
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Dec 5, 2025Locations: 1
Eligibility criteria

Age≥ 65 years old; [+2]

ASA classification≥ Class V; [+7]

Status: Recruiting

The Effect-site Concentration of Remifentanil Blunting Endotracheal Intubation Responses During Anesthesia Induction With Lidocaine or Sufentanil Combined With Etomidate: A Randomized Controlled Study

The aim of this study was to compare the effect-site target concentration (including EC₅₀ and EC₉₀) of remifentanil required to suppress cardiovascular responses to tracheal intubation during anesthesia induction with etomidate combined with either lidocaine or sufentanil.

Participants needed: 99
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Sep 22, 2025Locations: 1
Eligibility criteria

Patients scheduled for elective surgery under general anesthesia with endotrache... [+1]

Age <18 years or >65 years; [+9]

Status: Recruiting

Incidence of Postoperative Cognitive Decline in Patients With Preexisting Cognitive Impairment

This study aims to find out how often memory and thinking problems happen after surgery in people who already have memory issues before their operation. These memory problems are called postoperative cognitive decline (POCD). Older adults with memory problems before surgery may be more likely to have trouble with thinking, memory, and daily activities after their operation. This study will follow patients who already have memory problems before surgery and see how their thinking and memory change after surgery. The results will help doctors better understand how to care for these patients before, during, and after surgery.

Participants needed: 340
Trial details
Age: 60+Biological sex: AllType: ObservationalSponsor: Peking University Shenzhen HospitalUpdated: Aug 22, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Preexisting Cognitive Impairment (PreCI) Surgical Group [+3]

Expected difficulty in completing neuropsychological assessments (e.g., inabilit... [+9]

Status: Recruiting

A Prospective, Randomized Controlled Study of the Probiotics as Adjuvant Treatment for Bacterial Vaginosis

The investigators are trying to determine if oral Probiotics(Umeta-mimi,30 days) with Metronidazole vaginal suppositories (7 days) is better than using Metronidazole vaginal suppositories(7 days) only in preventing the recurrence of bacterial vaginosis

Participants needed: 140
Trial details
Phase: Phase 4Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Jun 12, 2025Locations: 1
Eligibility criteria

Aged 18 to 55 years old, with history of sexual activity, [+2]

History of systemic organic diseases or psychiatric diseases [+5]

Status: Recruiting

Treatment for Aerobic Vaginitis by Using Bofukang Vaginal Suppository

Aerobic vaginitis was treated by using Baofukang Suppository 7 days group or Baofukang Suppository 14 days group.To evaluate the efficacy and safety after treatment.

Participants needed: 50
Trial details
Phase: Phase 3Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Jun 12, 2025Locations: 1
Eligibility criteria

Vaginal dischareg ; [+2]

Patients with other vaginitis, cervical erosion, or suspected gonorrhea, herpes... [+5]

Status: Not yet recruiting

Study of Precision Treatment for Rare Tumours in China Guided by PDO and NGS

The objective of this Phase II, open-label, multicenter, non-randomised controlled clinical trial is to guide precision treatment for patients with rare tumours based on Patient-Derived Organoids/Next-Generation Sequencing drug screening.

Participants needed: 200
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Peking University Shenzhen HospitalUpdated: Nov 18, 2024
Eligibility criteria

Male or female, the age at the time of signing the informed consent is no less t... [+12]

No patient lesions available for organoid model construction; [+25]