Clinical trials

15

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

Condition / disease
Location
Status: Recruiting

High-flow Nasal Cannula Oxygen Therapy Versus Conventional Oxygen Therapy in High-altitude Pulmonary Edema

This study aims to evaluate whether High-flow Nasal Cannula Oxygen Therapy (HFNC) provides superior respiratory support compared to Conventional Oxygen Therapy (COT) in patients with High-Altitude Pulmonary Edema (HAPE).

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: May 4, 2026Locations: 1
Eligibility criteria

Aged 18 years or older; [+5]

Known or clinically confirmed pregnancy; [+10]

Status: Recruiting

Erythrocytapheresis for Chronic Mountain Sickness

The study aims to explore the efficacy and safety of erythrocytapheresis in chronic mountain sickness

Participants needed: 112
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Apr 2, 2026Locations: 1
Eligibility criteria

Age ≥18 years; [+11]

Status: Recruiting

Diagnostic Value and Safety of Combined Biopsy for Mediastinal Metastasis of Lung Cancer

The study is aimed o evaluate the diagnostic performance and treatment guidance of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) combined with transbronchial mediastinal cryobiopsy (EBUS-TBMCB) in patients with mediastinal metastases of lung cancer.

Participants needed: 240
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Mar 23, 2026Locations: 1
Eligibility criteria

Aged ≥18 years; [+1]

Presence of severe cardiopulmonary disease, coagulation disorders, massive hemop... [+5]

Status: Recruiting

Efficacy and Safety of Lubiprostone in the Treatment of Slow Transit Constipation

Lubiprostone has established efficacy and a favorable safety profile in chronic constipation and irritable bowel syndrome with constipation (IBS-C). However, clinical data specifically supporting its use in slow-transit constipation (STC), a distinct subtype of chronic constipation, remains limited.

Participants needed: 346
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Jan 20, 2026Locations: 15
Eligibility criteria

Patients voluntarily participated in the study and provided signed informed cons... [+6]

Pregnant or lactating women. [+14]

Status: Not yet recruiting

Effects of Compound Ejiao Syrup on Exercise Tolerance and Quality of Life in Critically Ill Patients After ICU Discharge: A Double-Blind, Multicenter,Randomized Controlled Clinical Study

This study, titled "Effect of Compound Ejiao Jiang on Exercise Tolerance and Quality of Life of Critically Ill Patients after Discharge from ICU: A Double-Blind, Multicenter, Randomized Controlled Clinical Study (LIFT Study)," intends to enroll 156 patients (78 in the experimental group and 78 in the control group). A double-blind design will be adopted, with patients receiving Compound Ejiao Jiang (20 ml each time, three times a day for 90 consecutive days) or a placebo for intervention. The primary outcome measure is the 6-minute walking distance on the 90th day after randomization. Meanwhile, secondary endpoints such as physical function, quality of life, and nutritional and inflammatory indicators will also be monitored. The aim of this study is to explore the rehabilitation value of Compound Ejiao Jiang for patients with post-intensive care syndrome (PICS) through high-level evidence-based medicine methods and to provide scientific evidence for the integrated traditional Chinese and Western medicine approach to improving the long-term prognosis of critically ill patients

Participants needed: 178
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Sep 5, 2025Locations: 1
Eligibility criteria

1. Obtain informed consent; 2. Age between 18 and 75 years (inclusive); 3. Disch...

1. Patients expected to die or for whom life-sustaining treatment will be withdr...

Status: Recruiting

Efficacy of Spironolactone Combined With Antihypertensive Drugs in Patients With Primary Aldosteronism

The goal of this observational study is to learn about the optimal dose of spironolactone treatment and the long-term outcomes on cardiovascular and cerebrovascular events in patients with lateralized PA who are unwilling to undergo surgery. The main question it aims to answer is: 1. What is the long-term effect of spironolactone treatment for lateralized PA? 2. What is the optimal dose of spironolactone treatment for the relief of renin inhibition in patients with lateralized PA? Participants will receive spironolactone treatment as part of their regular medical care for more than 12 months, and their clinical indicators, including blood pressure, biochemical remission, cardiovascular and renal damage, and the incidence of cardiovascular and cerebrovascular events, will be analyzed.

Participants needed: 350
Trial details
Age: 30-65Biological sex: AllType: ObservationalSponsor: Third Military Medical UniversityUpdated: Aug 22, 2025Locations: 1Duration: 12 Months
Eligibility criteria

Male or female, aged 30~65 years. [+3]

Hyperkalemia. [+10]

Status: Recruiting

Transcutaneous Auricular Vagus Nerve Stimulation as Adjuvant Treatment for Sepsis Patients

The goals of this randomized clinical trial are to investigate the effects of transcutaneous auricular vagus nerve stimulation (taVNS) combined with standard intensive care on systemic organ function in septic patients, and exploring its potential mechanisms for improving overall outcomes in sepsis.The main question it aims to answer is whether taVNS can reduce the severity of sepsis patients by ameliorating systemic inflammation.Participants will receive standard intensive care treatment and be randomized to receive the taVNS or sham taVNS as adjuvant treatment twice a day for 7 consecutive days. Several evaluations will be done before and after the intervention.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Jul 4, 2025Locations: 1
Eligibility criteria

Age 18-80 [+3]

severe ARDS defined by PaO₂/FiO₂ ≤100 mmHg with PEEP ≥5 cm H₂O [+9]

Status: Recruiting

PARLAR-02 Trial:Modified Transanal Drainage Tube Use for Preventing Anastomotic Leakage

Surgical resection remains the primary treatment for rectal cancer, but the postoperative incidence of anastomotic leakage (AL) is relatively high. AL not only increases the medical burden on patients, prolongs hospital stays, raises the need for secondary surgery, and elevates perioperative mortality, but also increases the long-term risk of local recurrence and reduces survival rates. There is an urgent need for a simple, effective treatment method that minimizes the burden on patients to prevent anastomotic leakage. The preoperative placement of a transanal drainage tube (TDT) is believed to effectively drain gas and feces from the intestinal lumen, thereby reducing intestinal pressure and alleviating tension at the anastomotic site, thus preventing AL. Previous studies have shown that traditional drainage tubes cannot effectively prevent leakage. Given the limitations of existing research on traditional TDTs, we plan to use a modified TDT (which allows postoperative irrigation and utilizes a balloon to block feces from adversely affecting the anastomosis) to conduct a randomized, parallel-controlled trial. This study aims to further investigate the role of the modified TDT in preventing and treating anastomotic leakage following rectal surgery

Participants needed: 968
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Jun 25, 2025Locations: 1
Eligibility criteria

Rectal adenocarcinoma (confirmed by pathology); [+7]

Emergency surgery; [+5]

Status: Recruiting

Comparison of Electrolyte Beverages and Water as Solvents for Bowel Preparation

Using Electrolyte Beverages as replacement for water to dissolve PEG(2L plan) in bowel preparation process. The aim of this study is to test whether Electrolyte Beverages as solvents can improve the cleanness of bowel preparation and the satisfaction of patients.

Participants needed: 2,766
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Mar 20, 2025Locations: 1
Eligibility criteria

Healthy individuals or those with mild or well-controlled chronic diseases. [+5]

Patients who refuse to participate in the study. [+10]

Status: Recruiting

Epidural Spinal Cord Stimulation for Lower-limb Impairment in Adrenomyeloneuropathy

Adrenal spinal neuropathy (AMN) is a rare X-linked genetic disease caused by mutations in the ABCD1 gene, and belongs to a special type of adrenal leukodystrophy. The patient's lower limb strength is weakened, the range of motion of the ankle joint is reduced, the hip flexors are weak and affect walking, and the peripheral nerves and vibration sensation are damaged. As the condition worsens, the lower limb muscle tone changes from hyperactivity to decrease, ultimately transitioning from spastic paralysis to flaccid paralysis. At present, the treatment plan for AMN is not yet perfect, and effective therapies are urgently needed to alleviate symptoms. Spinal cord electrical stimulation (SCS) is the implantation of a thin electrode into the epidural space of the corresponding spinal segment within the spinal canal. Then connect the electrodes to a nerve stimulator implanted subcutaneously in the iliac region, and use electrical pulses to stimulate the conduction of sensory neurons in the posterior column and posterior horn of the spinal cord for treatment, which can achieve the goal of controlling pain. In addition, SCS has also conducted research on the recovery of lower limb function in paraplegic patients and upper limb function in post-stroke hemiplegic patients, and has improved corresponding motor dysfunction to a certain extent. Spinal cord stimulation may be a potential treatment for motor dysfunction in AMN. Based on the above, this study attempts to evaluate the efficacy of SCS in treating lower limb muscle tone and movement disorders in AMN patients, and explore the potential therapeutic effects and related mechanisms of SCS on AMN. In this study, 10 AMN patients will be recruited. After enrollment, preoperative evaluation will be conducted. After preliminary assessment of motor function, neurological evaluation, and other related examinations, lumbar spinal nerve stimulators and pulse generators were implanted in our hospital. After the implantation surgery is completed, depending on the patient's recovery status, they will be transferred to various centers for subsequent rehabilitation treatment within one to two weeks, and then turned on for treatment. Before starting up, a second corresponding inspection and evaluation will be conducted. The third and fourth corresponding inspections and evaluations will be conducted one week and four weeks after startup, respectively. The patient will be discharged 4 weeks after starting up, and then return to the hospital for the fifth and sixth corresponding examinations and evaluations at 4 weeks and 6 months after discharge. Evaluate the effectiveness and safety of SCS in improving lower limb motor dysfunction in AMN patients through statistical analysis.

Participants needed: 10
Trial details
Age: 22-50Biological sex: MaleType: InterventionalSponsor: Third Military Medical UniversityUpdated: Jan 28, 2025Locations: 4
Eligibility criteria

Conforming to the diagnostic criteria of AMN, with a definite genetic testing re... [+3]

Other inherited diseases; [+9]

Status: Recruiting

Statin Combined with Amlodipine Treats Primary Aldosteronism

The drug treatment for primary aldosteronism (PA) is limited and difficult to improve long-term cardiovascular outcomes. This study plans to enroll patients with primary aldosteronism and randomly divide into 3 groups: scheme 1: Statin combined with amlodipine besylate, scheme 2: Statin combined with Spironolactone and Amlodipine besylate. scheme 3: Amlodipine besylate combined with Spironolactone , to observe the changes in plasma aldosterone level, 24-hour urinary aldosterone, blood pressure, and long-term cardiovascular risk.

Participants needed: 180
Trial details
Phase: Phase 4Age: 18-70Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Nov 22, 2024Locations: 1
Eligibility criteria

Clinical diagnosis of primary aldosteronism

Allergy to drugs in this study [+3]

Status: Recruiting

Effect of Bariatric Surgery Versus Medical Therapy on Metabolic Syndrome

Bariatric surgery (BS) is known to improve the components of metabolic syndrome (MS) in obese patients. However, few studies have evaluated the impact of bariatric surgery versus medical therapy (MT) in patients with MS, especially in patients with low body mass index (BMI). This study aimed to assess the effect of bariatric surgery on MS in patients with low BMI by comparing BS (BMI\<35 kg/m2 and BMI≥35 kg/m2) with MT (BMI\<35 kg/m2). A retrospective study including patients with MS undergoing bariatric surgery and medical therapy at a single institution. We follow up the 5 years effect of bariatric surgery versus medical therapy on the remission of MS, its individual components, atherosclerotic cardiovascular disease (ASCVD) risk, and medication used.

Participants needed: 200
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Third Military Medical UniversityUpdated: Aug 20, 2024Locations: 1Duration: 5 Years
Eligibility criteria

BMI<35 kg/m² [+2]

Patients who failed to follow up [+13]

Status: Recruiting

Effects of Adrenal Artery Ablation and Spironolactone in Patients With Primary Aldosteronism

Primary aldosteronism (PA) is one of the most common cause of endocrine and resistant hypertension. Current studies have shown that the activation of the renin-angiotensin-aldosterone system (RAAS) and the increased sympathetic nerve activity in the central or local tissue are the key mechanisms of high blood pressure and its organ damages. Current guidelines suggest that surgery and aldosterone receptor inhibitors are the only treatment for primary aldosteronism. However, only about 35% of aldosterone tumors and a small number of unilateral adrenal hyperplasia can be treated surgically. More than 60% of primary aldosteronism and bilateral adrenal hyperplasia need long-term oral aldosterone receptor inhibitors. At present, spironolactone is the most commonly used aldosterone receptor inhibitor. Long term use of spironolactone may cause hyperkalemia, hyperplasia of male mammary gland, hairiness of female and other adverse reactions. Therefore, the researchers suggest that partial removal of adrenals can reduce aldosterone level, lower blood pressure and restore potassium metabolism balance. In patients with primary hyperaldosteronism, the level of aldosterone increases, which can cause vascular endothelial dysfunction, myocardial injury and ventricular fibrosis. The study shows that long-term oral administration of spironolactone can reverse the above cardiovascular damage and correct heart failure. Adrenal artery ablation can reduce aldosterone level, but the long-term effect on cardiovascular system is unknown. In order to confirm the effect of adrenal artery ablation on blood pressure and cardiovascular system, the researchers conducted an open cohort study on patients with primary aldosteronism (including aldosterone, idiopathic aldosteronism and adrenal hyperplasia). To observe the effect of adrenal artery ablation and spironolactone on blood pressure, blood electrolyte, metabolic index, cardiovascular events and cardiovascular death risk in patients with primary aldosteronism, and to explore its efficacy and safety.

Participants needed: 60
Trial details
Age: 30-60Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Aug 20, 2024Locations: 1
Eligibility criteria

Primary Aldosteronis diagnosed by increased Renin ratio (ARR) and serum aldoster... [+3]

Aldosterone cancer. [+13]

Status: Not yet recruiting

A Study on Probiotic Formula in Autistic Children

A Randomized controlled double-blind clinical study on the effectiveness and safety of probiotic formula in Autistic children with gastrointestinal symptoms.

Participants needed: 156
Trial details
Age: 3-14Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: May 23, 2024Locations: 1
Eligibility criteria

Children and adolescents aged 3-11 years old [+3]

Antibiotics or probiotics used within 1 mont [+7]

Status: Recruiting

Neoadjuvant CIETAI With Concurrent Chemoradiotherapy in Local Advanced Rectal Cancer

To increase the efficacy of neoadjuvant PD-1/PD-1 checkpoint inhibitor in local advanced rectal cancer (LARC), we propose preoperative arterial infusion of Tirellizumab and oxaliplatin followed by tumor artery embolization with concurrent chemoradiotherapy as neoadjuvant regimen for LARC.

Participants needed: 90
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Third Military Medical UniversityUpdated: Aug 23, 2023Locations: 1
Eligibility criteria

Local advanced Rectal cancer: stage T3/4NanyM0 or T1-2N+M0. [+5]

Severe allergic reaction to humanized antibodies or fusion proteins; [+13]