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NCT ID: NCT06219031 Completed - Esophageal Cancer Clinical Trials

A Study of the Tumor Microenvironment Affecting the Efficacy of Immunotherapy for Esophageal Cancer

Start date: December 1, 2023
Phase:
Study type: Observational

This study is a retrospective study of clinical specimens. The study subjects were patients with esophageal cancer who received immunotherapy. Tumor tissue specimens surgically removed from patients before treatment will be collected primarily. In situ immunohistochemistry and multicolor immunofluorescence will be performed. We hypothesize that there are differences in lipid metabolism-related proteins in tumor tissues and immune cells in the preexisting tumor microenvironment in patients with esophageal cancer prior to immunotherapy, and that there is a link between such differences and the efficacy of immunotherapy.

NCT ID: NCT06218862 Completed - Clinical trials for ARDS Due to Disease Caused by SARS Co-V-2

Clinical Effects of Sivelestat Sodium on Improving ARDS in Patients With COVID-19

Start date: December 1, 2022
Phase:
Study type: Observational

The goal of this retrospective multicentre cohort study is to examine the association between receipt of sivelestat and improvement in oxygenation among patients with acute respiratory distress syndrome (ARDS) induced by COVID-19. We used propensity score matching to compare the outcomes of patients treated with sivelestat to those who were not. The primary outcome was the PaO2/FiO2 ratio on Day 3. Secondary outcomes included 28-day mortality, alive and ICU-free days within 28 days, non-mechanical ventilation time within 28 days, the lengths of stay in the ICU and hospital, proportion of patients requiring extracorporeal membrane oxygenation (ECMO), proportion of patients undergoing endotracheal intubation or tracheotomy, and incidence of adverse events (AEs) or severe adverse events (SAEs).

NCT ID: NCT06218160 Completed - Inguinal Hernia Clinical Trials

The Addition of Hydromorphone to Local Anesthetics for the Repair of Inguinal Hernias in Elderly Patients

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

To compare the clinical and postoperative analgesic effects of hydromorphone combined with ropivacaine and ropivacaine alone in quadrangular muscle block for open inguinal hernia in elderly patients.

NCT ID: NCT06215482 Completed - Clinical trials for Participants' Pain,Quality of Life and Hospital Satisfaction

The Effect of "Adjacent Bed Effect" Induced by Anxiety on the Perioperative Period of Patients With Chocolate Cyst of Ovary

Start date: July 22, 2023
Phase:
Study type: Observational [Patient Registry]

The "adjacent bed effect" caused by anxiety leads to poor recovery of participants after ovarian chocolate cyst surgery, including pain and quality of life, and affects participant satisfaction with the hospital.

NCT ID: NCT06214754 Completed - Clinical trials for Patients With Atherosclerotic Plaques in the Coronary Arteries That Require Excision

Efficacy and Safety of Intravascular High-pressure Cutting Balloon Catheters for PCI

Start date: June 16, 2023
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the safety and efficacy of intravascular high-pressure cut balloon catheter compared to cut balloon catheter during PCI, and to support product registration and clinical application.

NCT ID: NCT06214481 Completed - Atopic Dermatitis Clinical Trials

A Study to Evaluate Rocatinlimab (AMG 451) in Healthy Chinese Participants

Start date: January 23, 2024
Phase: Phase 1
Study type: Interventional

The primary objective of the study is to evaluate the pharmacokinetics of rocatinlimab after single subcutaneous (SC) administration in healthy Chinese participants.

NCT ID: NCT06214247 Completed - Clinical trials for Coronary Artery Disease

Wedge NC - Scoring Balloon Dilatation Catheter

Start date: August 27, 2021
Phase: N/A
Study type: Interventional

To evaluate the efficacy and safety of Wedge NC Scoring Balloon Dilatation Catheter for dilating coronary stenosis during PCI in comparison with a similar product on the market.

NCT ID: NCT06213870 Completed - Clinical trials for Endovascular Thrombectomy

Screening of Endovascular Thrombectomy With MRI in Acute Ischemic Stroke

Start date: August 1, 2022
Phase:
Study type: Observational

The goal of this observational study is to learn about the role of MRI evaluation based on FVH-DWI mismatch principle in preoperative evaluation of endovascular thrombolectomy. The main questions it aims to answer are: - The consistency between MRI and perfusion examination in determining EVT indications. - The consistency of functional independence rate between patients screening with MRI and perfusion.

NCT ID: NCT06213727 Completed - Clinical trials for Corneal Epithelial Defect

ZKY001 Eye Drops in the Treatment of Corneal Epithelial Defects in a Phase Ⅱ Clinical Trial

Start date: March 15, 2022
Phase: Phase 2
Study type: Interventional

A multicenter, randomized, double-blind, placebo-controlled clinical trial was designed. The study included two experimental groups (low-dose ZKY001 eye drops group and medium-dose ZKY001 eye drops group) and a placebo control group, with 60 subjects in each group.

NCT ID: NCT06213597 Completed - Stroke Clinical Trials

Effects of Repetitive Transcranial Magnetic Stimulation on Patients With Dysphagia in Stroke Observed Based on Functional Near-infrared Spectroscopic

Start date: May 28, 2023
Phase: N/A
Study type: Interventional

This trial was a randomized, double-blind, sham-controlled trial.Thirty patients with post-stroke dysphagia were randomly assigned to the repetitive transcranial magnetic stimulation(rTMS) group (n=15) or sham rTMS group (n=15). Both groups received conventional swallowing rehabilitation, and in addition, the rTMS group received 5hz repetitive transcranial magnetic stimulation on the healthy side. Swallowing function was assessed at admission and after two weeks of treatment using the the Standardized Swallowing Assessment (SSA), the Penetration-Aspiration Scale (PAS), the Fiberoptic Endoscopic Dysphagia Severity Scale(FEDSS), the Functional Oral Intake Scale (FOIS), and the functional near-infrared spectroscopic(fNIRS).