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Syndrome clinical trials

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NCT ID: NCT02627573 Terminated - Clinical trials for Myelodysplastic Syndromes

Trial of GVHD Prophylasxis With PTCy or Thymoglobulin in Unrelated SCT

Start date: July 2015
Phase: Phase 2
Study type: Interventional

Purpose There is a growing evidence of high efficacy of post-transplantation cyclophocphomide (PTCy)-based GVHD prophylaxis in haploidentical and matched related and unrelated bone marrow transplantation. There is limitted, but growing data on safety and efficacy of this prophylaxis in unrelated and peripheral blood stem cell transplantations. Use of PTCy in chronic myeloproliferative neoplasms and myelodisplatic syndrome is of particular interest. On the one hand, PTCy could reduce the incidence of chronic GVHD and long-term bormidity. On the other hand, there is a concern, that PTCy can increase the incidence of graft failures in this group of patients. Currently published data indicate that low-dose Thymoglobulin-based prophylaxis is the most promissing compatitor in terms of acute and chronic GVHD control. So there is a rationale to randomize Thymoglobulin and PTCy as GVHD prophilaxis. Pre-transplant assesment of moratlity (PAM)-index will be used as the strata for randomization, as it is the paramter that takes into account the most important factors effecting survival. The conditioning regimen and the other two components of GVHD prophylaxis (mycophenolate mofetil and tacrolimus) will be identical in the two arms of the study.

NCT ID: NCT02626741 Recruiting - Clinical trials for Abdominal Obesity-Metabolic Syndrome

Effect of a Meal Replacement on Weight Loss Obesity Patients With Metabolic Syndrome

SlimWell
Start date: February 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether meal replacement, SlimWell ®, is effective in the treatment of obesity patients with metabolic syndrome.

NCT ID: NCT02626663 Withdrawn - Clinical trials for Thrombotic Thrombocytopenic Purpura

The Role of Microparticles as a Biomarker

Start date: July 2016
Phase:
Study type: Observational

The investigators propose to characterize MPs in aHUS and TTP both at the onset and throughout treatment. The investigators believe that the number, size, and cell origin of MPs will differ between these two diseases. The hypothesis is that endothelial derived MPs will be higher in number and comprise a larger portion of the MP population in aHUS and that platelet MPs will comprise a larger number and greater proportion of MPs in TTP. The investigators believe that MP identity and number can be used to reliably differentiate between aHUS and TTP at disease onset.

NCT ID: NCT02625064 Not yet recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Discovery of New Early Detection Biomarkers of Acute Respiratory Distress Syndrome

ARDS
Start date: January 2016
Phase: N/A
Study type: Observational

The goal of this project is to find a series novel biomarkers by differential proteomic techniques that can improve the early diagnosis and develop a more efficient therapy to enhance ARDS patient survival rate.

NCT ID: NCT02623777 Completed - Metabolic Syndrome Clinical Trials

Effect of Arabinoxylan Oligosaccharides Consumption on Insulin Resistance in Patients With Metabolic Syndrome

Start date: March 2015
Phase: N/A
Study type: Interventional

During this project the investigators will evaluate whether the effects of arabinoxylan oligosaccharides (AXOS) consumption on insulin resistance in participants with metabolic syndrome can be explained by the production of short-chain fatty acids (SCFA). Secondly, the investigators will evaluate whether changes in gut hormone production might explain the effect on insulin resistance.

NCT ID: NCT02623192 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Respiratory Mechanics Registry for ARDS Patients

Start date: August 2014
Phase: N/A
Study type: Observational [Patient Registry]

This registry was proposed to investigate the epidemiology of respiratory mechanics in patients with ARDS through collecting data from a QI project which was constituted with systematic assessments of respiratory mechanics and gas exchange.

NCT ID: NCT02622724 Terminated - Clinical trials for Respiratory Distress Syndrome, Adult

Efficacy and Safety of FP-1201-lyo (Interferon Beta-1a) in Patients Having Acute Respiratory Distress Syndrome (ARDS)

INTEREST
Start date: December 23, 2015
Phase: Phase 3
Study type: Interventional

In this study effectiveness and safety of a new drug FP-1201-lyo (recombinant human interferon beta-1a) is compared to placebo. Investigation is conducted with patients who have acute respiratory distress syndrome (ARDS). The new drug is expected to reduce the time which a patient need to be on the ventilator and improve patient's chances of survival. Currently there are no approved drugs for treating moderate or severe ARDS patients.

NCT ID: NCT02621892 Completed - Clinical trials for Constipation Predominant Irritable Bowel Syndrome

A 12-Week Study With a 4-Week Randomized Withdrawal Period to Evaluate the Efficacy and Safety of Tenapanor for the Treatment of IBS-C

T3MPO-1
Start date: October 2015
Phase: Phase 3
Study type: Interventional

This phase 3, 12-week, randomized, double-blind, placebo-controlled, multi-center study will evaluate the safety and efficacy of tenapanor in subjects with constipation-predominant irritable bowel syndrome (IBS-C) as defined by the ROME III criteria and who have active disease as determined after a two-week screening period. Subjects who qualify and are randomized into the study will either receive 50mg BID of tenapanor or placebo BID for 12 week treatment period and then undergo a 4 week placebo controlled randomized withdrawal.

NCT ID: NCT02621567 Completed - Clinical trials for Depressive Symptoms Post Cardiac Surgery or Post Acute Coronary Syndrome

Bright Light Therapy Efficacy for Depressive Symptoms Following Cardiac Surgery or Acute Coronary Syndrome: Pilot Trial

BEAM-P
Start date: January 2016
Phase: Phase 4
Study type: Interventional

Bright Light Therapy Efficacy for Depressive Symptoms Following Cardiac Surgery or Acute Coronary Syndrome: Pilot Trial (BEAM-P) is a randomized controlled trial (RCT) that seeks to assess the feasibility of conducting a full trial which would assess the efficacy of Bright Light Therapy (BLT) for improving depressive symptoms post-cardiac surgery or acute coronary syndrome.

NCT ID: NCT02620605 Recruiting - Clinical trials for Ovarian Hyperstimulation Syndrome

The Influence of Timing of Cabergoline Initiation on Prevention of OHSS

OHSS
Start date: December 20, 2017
Phase: Phase 3
Study type: Interventional

Study the effect of early cabergoline administration in prevention of occurrence or decreasing the severity of OHSS in patients undergoing intra cytoplasmic sperm injection.And its effect on oocyte maturation,fertilization and pregnancy rate..