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NCT ID: NCT05877651 Completed - Solid Tumors Clinical Trials

MASCT-I in Patients With Metastatic or Recurrent Solid Tumors Who Failed Standard Therapy.

Start date: April 21, 2020
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of MASCT-I in patients with metastatic or recurrent solid tumors who failed standard therapy.

NCT ID: NCT05876793 Completed - Effect of Drug Clinical Trials

Effective Dose of Remimazolam Combined With Propofol in Painless Gastroscopy

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

This study used sequential method(Dixon's up and douwn) to determine the effective dose of remiazolam combined with propofol in painless upper gastrointestinal endoscopy

NCT ID: NCT05875662 Completed - Clinical trials for Mechanical Ventilation

Pulmonary Ventilation After Fiberoptic Bronchoscopy Using EIT

Start date: May 5, 2023
Phase:
Study type: Observational

Background: Fiber bronchoscopy is a routine operation in intensive care unit (ICU), but it may cause local collapse of the lung. Recruitment maneuver (RM) after fiber bronchoscopy may have the potential to restore functional residual air volume and increase lung volume. However, there is still a lack of quantitative indicators to evaluate the effect of recruitment maneuver. With electrical impedance tomography (EIT), we can monitor lung ventilation in real time to understand the situation of lung ventilation. Objective: To evaluate whether recruitment maneuver after fiber bronchoscopy can improve lung volume and improve lung ventilation, and which people are most likely to benefit from it, by monitoring the end expiratory pulmonary impedance of critically ill patients undergoing bedside fiber bronchoscopy to monitor the lung ventilation before and after the operation and before and after recruitment maneuver. Study Design: A prospective observational study was conducted to monitor the end expiratory lung impedance (EELI), tidal impedance variable (TIV), global inhomogeneity (GI) index and Center of Ventilation (CoV) before and after bronchoscopy and recruitment maneuver, and then to understand the changes of lung volume and ventilation.

NCT ID: NCT05875584 Completed - Colorectal Cancer Clinical Trials

Exploratory Study of a Novel Based rbcDNA Liquid Biopsy Technique for Colorectal Cancer Early Detection

Start date: May 18, 2023
Phase:
Study type: Observational

Exploration of a novel rbcDNA liquid biopsy technique for early detection of colorectal cancer is a promising development in the field of disease diagnosis and screening. This technique has the potential to establish an efficient and sensitive system for the early detection of colorectal cancer, which can provide a new perspective for individual health monitoring.

NCT ID: NCT05875493 Completed - Clinical trials for Food Effect in Healthy Participants

A Food Effect Study of JAB-21822 in Healthy Subjects

Start date: May 12, 2023
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to determine the effect of food in healthy participants on the bioavailability of JAB-21822 following single dose administration with and without a meal

NCT ID: NCT05874622 Completed - Clinical trials for Rheumatoid Arthritis

A Phase I Clinical Study of VC005 Tablets in Subjects With Rheumatoid Arthritis.

Start date: June 12, 2023
Phase: Phase 1
Study type: Interventional

This is a randomized, double-blind, dose-escalating, placebo-controlled phase Ib clinical study.

NCT ID: NCT05874518 Completed - Electroacupuncture Clinical Trials

Clinical Observation of Warm Needling Combined With and Electroacupuncture Therapy on Ovulatory Dysfunction

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

To observe the effect of warm needling combined with electroacupuncture on the ovulation promotion rate and pregnancy rate in luteinized unruptured follicle syndrome (LUFS).

NCT ID: NCT05873426 Completed - Pharmacokinetics Clinical Trials

Mass Balance Study of [14C]ZSP1273 in Healthy Adult Male Subjects in China

Start date: March 25, 2023
Phase: Phase 1
Study type: Interventional

This study is a single-center, open-label, and single-dose clinical study to evaluate the mass balance, biotransformation and pharmacokinetics of [14C]ZSP1273 in healthy Chinese male participates, revealing the overall pharmacokinetic characteristics of ZSP1273.

NCT ID: NCT05873348 Completed - COVID-19 Infection Clinical Trials

A Controlled Study on Regulation of Systemic Inflammation by Fecal Bacteria Transplantation in Patients With COVID-19.

Start date: January 10, 2023
Phase: N/A
Study type: Interventional

A total of 30 hospitalized patients with COVID-19 over 60 years old were enrolled in this study and were divided into the experimental group (n=15) and the control group (n=15) at a ratio of 1:1. Both groups were treated according to the 2022 Shanghai guidelines for Diagnosis and Treatment of COVID-19 infection and the hierarchical diagnosis and treatment process. The experimental group was treated with fecal microbiota transplantation (FMT) capsules for 1 week, and the control group was treated with empty capsules. Patients in both groups were followed up for 1 month after discharge. To observe the effect of combined FMT capsule treatment on the regulation of inflammatory factors in peripheral blood and the remodeling of intestinal flora, and to verify its safety.

NCT ID: NCT05872425 Completed - PCOS Clinical Trials

Efficacy and Safety of Dingkundan Combined With Combination Oral Contraceptives in the Treatment of PCOS

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

This is a single-center, non-randomized, open-label clinical study to investigate the efficacy and safety of Dingkundan (DKP) combined with compound oral contraceptives (COC) in the treatment of PCOS. This study is mainly to compare the effect of COC plus DKP verse COC on reducing androgen, improving the function of ovarian and the individual metabolism. The secondary objective of our study is to explore the efficacy of DKP on pregnancy in patients with PCOS and its safety.