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NCT ID: NCT05885737 Active, not recruiting - Uremic Pruritus Clinical Trials

Phase 3 Study of Difelikefalin in Haemodialysis Chinese Adult Subjects With Moderate-to-Severe Pruritus

Start date: May 30, 2023
Phase: Phase 3
Study type: Interventional

This a multicentre study that consists of a 12-week double-blind period, and an optional 14-week open-label extension period and a 1-week follow-up period.

NCT ID: NCT05882305 Active, not recruiting - Clinical trials for EBV-associated Lymphomas

KSD-101 Therapy for EBV-associated Lymphomas: an Exploratory Clinical Trial

Start date: June 10, 2023
Phase: Early Phase 1
Study type: Interventional

The main purpose of this study is to determine the tolerability and feasibility of KSD-101 in patients with EBV-associated haematologic neoplasms,to observe the characteristics of dose-limiting toxicity (DLT)and to explore the range of effective dose.

NCT ID: NCT05882214 Active, not recruiting - Hepatic Steatosis Clinical Trials

Metabolic Changes Induced by NMN in Healthy Subjects With Acute Binge Drink

NMN-MeABD
Start date: March 1, 2024
Phase: N/A
Study type: Interventional

The goal of this double-blinded, randomized, crossover trial is to investigate the effects of NMN supplementation on liver function, liver fat content and lipid metabolism in healthy young subjects with acute binge drink. The main questions it aims to answer are: 1. if NMN administration could accelerate alcohol metabolism and alleviate hangover symptom; 2. if NMN administration could alleviate alcohol-induced liver injury and hepatic steatosis.

NCT ID: NCT05881837 Active, not recruiting - Clinical trials for Overweight or Obesity

Efficacy and Safety of HRS9531 Injection in Obese Subjects Without Diabetes

Start date: June 13, 2023
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and dose-response relationship of HRS9531 injection compared with placebo in reducing body weight in obese subjects without diabetes after 24 weeks of treatment.

NCT ID: NCT05881785 Active, not recruiting - Clinical trials for Axial Spondyloarthritis

Study of Efficacy and Safety of GR1501 in Patients With Radiographic Axial Spondyloarthritis

Start date: June 13, 2022
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to demonstrate the clinical efficacy of GR1501 at week 16; and to demonstrate safety and tolerability of GR1501 compared to placebo in patients with Radiographic Axial Spondyloarthritis at week 16 and long term safety up to Week 48。 The main question it aims to answer is whether GR1501 injection was superior to placebo in the proportion of subjects with ASAS20 response at week 16 in patients with Radiographic Axial Spondyloarthritis.

NCT ID: NCT05880485 Active, not recruiting - Clinical trials for Uterine Cervical Neoplasm

Online Adaptive Radiotherapy Cervical Cancer With Reduced Margin for Cervical Cancer

Start date: February 2, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Online adaptive radiotherapy (oART) has demonstrated to be feasible to reduce planning target volume (PTV) margins for cervical cancer. To explore the value of reduced margins in oART for cervical cancer, we conducted a prospective clinical trial to determine the clinical efficacy and toxicity of reduced margins.

NCT ID: NCT05878093 Active, not recruiting - Clinical trials for Chronic Rhinosinusitis With Nasal Polyps

Dupilumab in Chinese Adult Participants With CRSwNP

Start date: May 16, 2023
Phase: Phase 3
Study type: Interventional

This is a parallel group, Phase 3, 2-arm study for treatment. The purpose of this study is to evaluate dupilumab subcutaneous (SC) injections compared to placebo in Chinese adult participants with CRSwNP, on a background therapy with intranasal corticosteroids (budesonide nasal spray). Study details include: - The study duration will be up to 40 weeks. - The treatment duration will be up to 24 weeks. - The number of visits will be 7.

NCT ID: NCT05877625 Active, not recruiting - Clinical trials for Ventilator-associated Pneumonia

Study on Dynamic Environmental Exposome of ICU and the Establishment of Microbial Transmission Model Between Environment and Host

Start date: August 1, 2022
Phase:
Study type: Observational [Patient Registry]

HAI (Hospital-acquired infection) is very common in ICU,and lack of understanding of environmental exposure omics and environment-host microbial interactions restricts the prevention and control of HAI. In this project, the investigators try to analyze the spatial and temporal distribution characteristics and evolution of microorganisms and their functions in the ICU environment through metagenome.

NCT ID: NCT05875909 Active, not recruiting - Clinical trials for Myopia, Degenerative

Corneal Flap Transplantation for Macular Hole Repair of High Myopia

Start date: February 23, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to learn about an innovative surgical technique for macular hole repair. This technique is for patients with high myopia using pars plana vitrectomy (PPV) combined with corneal flap transplantation. The main questions it aims to answer are: - Is the innovative surgical technique useful for patients? - Is the surgical technique safe for patients? Participants will: - Undergo PPV combined with corneal flap transplantation to cover the macular hole. - Maintain a prone position for 2 weeks postoperatively. - Be observed by visual acuity, slit lamp, optical coherence tomography (OCT) and fundus photography for 1 year after surgery.

NCT ID: NCT05874752 Active, not recruiting - Clinical trials for Coronary Artery Disease

Myocardial Function Assessment in Patients With Coronary Artery Disease Using Noninvasive Myocardial Work

Start date: October 1, 2021
Phase:
Study type: Observational

Noninvasive pressure-strain loop (PSL) derived myocardial work (MW) are more sensitive than conventional echocardiographic parameters in quantitative assessment of early myocardial dysfunction. The aim of this study was to assess left ventricular (LV) myocardial function in symptomatic patients with coronary artery disease using the promising method. Methods: Transthoracic echocardiography was performed on patients with angina or equivalent symptoms before coronary angiography. Images were stored and imported into the software for further offline analysis of PSL-based MW. MW analysis were carried out on each patient for global and regional myocardial function assessment.