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NCT ID: NCT05037357 Recruiting - Clinical trials for Nasopharyngeal Carcinoma

Verification of Harmonization of Plasma Epstein-Barr Virus DNA Measurements

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

Plasma Epstein-Barr virus (EBV) DNA will be measured in native plasma samples of nasopharyngeal carcinoma (NPC) patients, respectively, by three medical centers and a qualified laboratory in Southern China, the highest endemic area of NPC. Passing-Bablok regression and difference plots will be used to compare results from each center to the all-method median and mean values. Agreement among methods will be evaluated against bias derived from a biological variation.

NCT ID: NCT05037045 Recruiting - Clinical trials for Type 2 Diabetes Mellitus

Effect of Gene Polymorphisms on GLP-1 Receptor Agonists Response in Patients With T2DM

Start date: January 10, 2019
Phase: N/A
Study type: Interventional

1. This is an prospective study to evaluate the effect of gene polymorphisms on therapeutic responses to glucagon like peptide-1 receptor agonist (GLP-1 RA) in patients with T2DM. 2. T2DM patients and healthy subjects were recruited to identify genotypes and detect the level of T2DM susceptibility genes expression levels in the plasma of healthy participants and T2DM patients. 3. This is a retrospective cohort study of patients with T2DM who were treated with exenatide twice daily as a part of their diabetes care for at least 12 months.

NCT ID: NCT05036928 Recruiting - HIV Infections Clinical Trials

Study of MDW Levels Predicting the Development of Sepsis in Hospitalized HIV-infected Patients and Correlation With Prognosis

Start date: December 2021
Phase:
Study type: Observational

Sepsis is a common and critical complication in HIV-infected patients and an important marker of high risk of patient death. The widely used diagnostic criteria for sepsis still have many deficiencies and do not allow for good prediction and timely determination of the onset of sepsis. In HIV-infected patients, abnormal activation of monocyte-macrophage is also a key mechanism in the development of their sepsis. Monocyte distribution width (MDW) is a marker of the degree of peripheral blood monocyte activation and has been recommended abroad for the early diagnosis of adult sepsis patients in emergency departments. However, in China, MDW has not been applied to the clinic yet, and the related studies are almost blank. Therefore, it is worthwhile to analyze the monocyte activation status of HIV-infected patients by MDW assay and thus predict the occurrence of sepsis.

NCT ID: NCT05036850 Recruiting - Kidney Diseases Clinical Trials

China Kidney Patient Trials Network

CKPTN
Start date: September 27, 2021
Phase:
Study type: Observational [Patient Registry]

This is a prospective multi-centre, observational cohort study of incident and prevalent patients diagnosed with a kidney disease in China.

NCT ID: NCT05036759 Recruiting - Atherosclerosis Clinical Trials

68Ga-FAPI PET/MR for Atherosclerosis

Start date: May 26, 2021
Phase: Early Phase 1
Study type: Interventional

A thin-cap fibroatheroma with a large necrotic core and macrophage infiltration marks the vulnerable plaque. Fibroblast activating protein (FAP) is an active serine protease, which can degrade type I collagen, potentially thinning the fibrous cap. Thus we speculate that atherosclerotic plaque could be imaged with 68Ga-FAPI PET/MR.

NCT ID: NCT05036473 Recruiting - Parkinson Disease Clinical Trials

A Study of the Efficacy and Safety of Carbidopa-Levodopa Extended-Release Tablets in Patients With Parkinson's Disease

Start date: October 12, 2021
Phase: Phase 2
Study type: Interventional

It is a phase II randomized, parallel, double-blind, placebo-controlled, multi-center clinical trial of the efficacy and safety of WD-1603 Carbidopa-Levodopa Extended-Release Tablets in patients with Parkinson's disease. The objective of the study is to access the safety and efficacy of WD-1603 carbidopa-levodopa extended-release tablets in patients with Parkinson's disease.

NCT ID: NCT05036395 Recruiting - Neonatal Seizure Clinical Trials

The Effect of AI-assisted cEEG Diagnosis on the Administration of Antiseizure Medication in Neonatal Seizures

Start date: March 16, 2022
Phase: N/A
Study type: Interventional

This is a prospective randomised clinical trial study to test an artificial intelligence (AI)-assisted continuous electroencephalogram(cEEG) diagnostic tool for optimizing the administration of antiseizure medication (ASM) in neonatal intensive care units(NICUs).

NCT ID: NCT05035914 Recruiting - Clinical trials for Advanced Colorectal Cancer

Anlotinib Combined With mXELIRI as Second-line Treatment of Advanced Colorectal Cancer

Start date: July 9, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

1. Determine the maximum tolerable dose (MTD) and / or phase II recommended dose (RP2D) of the allotinib combined mXELIRI protocol. 2. To evaluate the safety and tolerance of the combination of anlotinib and mXELIRI in the second-line treatment of patients with advanced colorectal cancer

NCT ID: NCT05035797 Recruiting - Critical Illness Clinical Trials

CaRe-ECMO Program on ECMO Weaning

CaRe-ECMO
Start date: October 15, 2021
Phase: N/A
Study type: Interventional

Mortality of patients suffering critical illness has been dramatically improved with advanced technological development of extracorporeal membrane oxygenation (ECMO) therapy. However, weaning rate stayed low in a majority of ECMO-supported patients. As one of several options, cardiopulmonary rehabilitation serves as effective intervention in the improvement of cardiovascular and respiratory function in various major critical illness. Nonetheless, its roles in facilitating ECMO weaning has not yet been explored. The purpose of this study is to investigate the effectiveness of cardiopulmonary rehabilitation on rate of ready for weaning in ECMO-supported patients (CaRe-ECMO).

NCT ID: NCT05035498 Recruiting - Clinical trials for Hemodynamic Instability

Prophylactic Norepinephrine and Phenylephrine Infusion for Hemodynamic Effects in Patients With Preeclampsia

Start date: February 1, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the maternal cardiac output response to prophylactic norepinephrine and phenylephrine infusion for postspinal anesthesia hypotension in parturients with preeclampsia undergoing cesarean section.