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NCT ID: NCT04103996 Completed - Respiratory Failure Clinical Trials

Incidence, Risk Factors and Outcomes of Diaphragm Dysfunction After Lung Transplantation

RADAR
Start date: February 10, 2020
Phase:
Study type: Observational

The study is designed to characterize the changes in diaphragm function after lung transplantation.

NCT ID: NCT04103905 Completed - Clinical trials for CD20-positive B Cell Non-Hodgkin Lymphoma

A Study of MIL62 in Treatment of CD20 Positive B-cell Lymphomas

Start date: February 10, 2017
Phase: Phase 1
Study type: Interventional

This open-label, multicenter,dose-escalating phase I study was designed to evaluate the safety, tolerability, pharmacokinetics and efficacy of MIL62 in Chinese patients with relapsed/refractory CD20-positive B-cell non-Hodgkin lymphoma(NHL) for whom no treatment of higher priority was available.

NCT ID: NCT04103892 Completed - Clinical trials for Adjunctive Treatment of Major Depressive Disorder

A Study of CLE-100 (Oral Esketamine) in Addition to Standard Antidepressant Drug for Major Depressive Disorder - CLEO Study

Start date: September 5, 2019
Phase: Phase 2
Study type: Interventional

The clinical trial is a Phase 2, double-blind, randomized, placebo controlled study in Major Depressive Disorder (MDD) participants currently treated with antidepressant therapy. The objective of the study is to assess CLE-100 for the treatment of MDD in participants currently treated with standard antidepressant therapy.

NCT ID: NCT04103801 Completed - Pain, Acute Clinical Trials

Substance P as a Biomarker to Evaluate the Reduction of Multiple Immunization Pain

Start date: July 14, 2017
Phase: N/A
Study type: Interventional

Immunization is one of the most significant preventive health measures in reducing morbidity and mortality caused by infectious diseases. Studies have shown that Sucrose is recommended to reduce pain associated with vaccination in neonates. The main aim of the study was to determine the effectiveness of sucrose in reducing infant's pain outcomes during immunization among 10-24 month-old infants and toddlers.

NCT ID: NCT04103749 Completed - Clinical trials for Endoscopic Retrograde Cholangiopancreatography

Global Prospective Case Series Using a Single-Use Duodenoscope

Start date: March 22, 2021
Phase: N/A
Study type: Interventional

Confirm procedural performance of the ExaltTM Model D Single-Use Duodenoscope in Endoscopic Retrograde Cholangio-Pancreatography (ERCP) and other duodenoscope-based procedures

NCT ID: NCT04103632 Completed - Adolescent Clinical Trials

Screening and Diagnosing Exercise-induced Bronchoconstriction in Recreational Young Athletes (12-18 y)

Start date: October 23, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to validate the screening protocol to study risk factors of exercise-induced bronchoconstriction (EIB) obtained in our previous study in high-school elite athletes (NCT03587675), in recreational young athletes who perform intense physical exercise.

NCT ID: NCT04103541 Completed - Clinical trials for Children Exposed to Adverse Experiences

Epigenetic Impact of a Psychotherapeutic Program in Adolescents With Severe Adverse Experiences

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

In this project, the investigator proposes to examine the influence of a psychotherapeutic program, designed for adolescents with a history of early adverse environmental and psychosocial experiences, on gene expression in order to find ways to reverse critical molecular mechanisms that associate extreme childhood stress with the development of a series of health problems, with important repercussions at both the individual and social levels.

NCT ID: NCT04103489 Completed - Preeclampsia Severe Clinical Trials

The Use of Eculizumab in HELLP Syndrome

Start date: February 23, 2021
Phase: Phase 1
Study type: Interventional

This research study is being performed to see if women diagnosed with early preterm Hemolysis, Elevated Liver Enzymes, Low Platelets (HELLP) syndrome (estimated gestational ages of 23-30 weeks) benefit from a medication called eculizumab (ECU). This drug blocks a part of the immune system called complement. By blocking this part of the immune system, eculizumab may stop or reverse the progression of the HELLP syndrome disease. The investigators will also look to see if this drug is effective and benefits both the mother and fetus.

NCT ID: NCT04103333 Completed - Angelman Syndrome Clinical Trials

Angelman Syndrome (AS) Biomarker Study

Start date: December 18, 2019
Phase: Early Phase 1
Study type: Interventional

The primary objective of this study is to measure ubiquitin-protein ligase E3A (UBE3A) protein levels in cerebrospinal fluid (CSF) and to evaluate its utility as a biomarker in support of the development of therapies for AS.

NCT ID: NCT04103229 Completed - Clinical trials for Urine Leakage in the Indwelling Urinary Catheterization

Urinary Leakage in the Indwelling Urinary Catheterization

Start date: April 1, 2015
Phase: N/A
Study type: Interventional

In the indwelling urinary catheterization (IUC), urinary leakage may develop around the catheter in the following days of catheterization. The volume and type of fluid used to inflate the catheter balloon has the potential to be a factor in the development of this problem. In this study, the investigators aimed to investigate the effect of the type and amount of fluid used in inflating the silicone foley catheter balloon on the development of urinary leakage around the catheter. In addition to purpose, the following questions were answered to determine the optimal solution type and volume in inflating the balloon: - What was the incidence of urinary leakage in IUC? - Was there a relationship between catheterization time and urine leakage? - Was there a relationship between the type of fluid used to inflate the foley catheter balloon and urine leakage? - Was there a relationship between the amount of fluid used to inflate the foley catheter balloon and urine leakage?