Clinical Trials Logo

Syndrome clinical trials

View clinical trials related to Syndrome.

Filter by:

NCT ID: NCT03252249 Completed - Clinical trials for Coronary Artery Disease

Duration of Dual Anti-Platelet Therapy (DUAL-ACS)

Start date: April 26, 2018
Phase: Phase 4
Study type: Interventional

Despite substantial evidence supporting the use of dual anti-platelet therapy in patients with acute coronary syndrome, there remains major uncertainty regarding the optimal duration of therapy. Recent evidence suggests that shorter durations of dual anti-platelet therapy are superior because the avoidance of atherothrombotic events is counterbalanced by the greater risks of excess major bleeding with apparent increases in all-cause mortality with longer durations. We here propose an international randomised controlled trial of 18,318 patients with type 1 myocardial infarction allocated to differing durations of dual anti-platelet therapy. We will use electronic health record linkage to track duration of therapy and clinical outcomes in a real-world, real-time, efficient and highly cost-effective trial. This has the potential to define treatment duration, settle a major outstanding international controversy, and influence modern cardiology practice across the world.

NCT ID: NCT03252223 Completed - Healthy Clinical Trials

Ovarian Response to Recombinant Follicle Stimulating Hormone in Women With PCOS

Start date: October 2, 2017
Phase: Phase 4
Study type: Interventional

Women with PCOS suffer from anovulation and, as a result, infertility. Efforts to clinically induce ovulation in these women using follicle stimulating hormone (FSH) administered subcutaneously seemingly requires prolonged administration compared to that of ovulatory women without PCOS. The apparent differing ovarian responsiveness to FSH between PCOS and normal women has not been carefully studied. We propose to address this issue by performing a dose-response study and examine ovarian follicle (estrogen, E2) responses to FSH administered subcutaneously in women with PCOS compared to responses observed in normal women.

NCT ID: NCT03252041 Not yet recruiting - Clinical trials for Pelvic Pain Syndrome

MRI & MRV in Pelvic Congestion Syndrome in Females

PCS
Start date: September 1, 2017
Phase: N/A
Study type: Observational

To investigate the feasibility of MRI and MRV in diagnosis of pelvic congestion syndrome.

NCT ID: NCT03251716 Completed - Schizophrenia Clinical Trials

Berberine Treat Metabolic Syndrome in Schizophrenia

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

In early clinical study investigators confirmed that berberine could prevent glucose and lipid metabolism disorder in schizophrenia, so investigators intend to verify the effect and safety of berberine in treatment for metabolic syndrome in schizophrenia.

NCT ID: NCT03251625 Completed - Clinical trials for Irritable Bowel Syndrome

Multi-strain Probiotic in the Management of IBS-D

Start date: April 2015
Phase: Phase 4
Study type: Interventional

1. To assess the effect of multistrain probiotics on abdominal pain using a validated symptom severity score in IBS patients. 2. To assess the efficacy of a multi-strain probiotic supplement as a treatment option for IBS in a tertiary referral centre

NCT ID: NCT03251300 Recruiting - Clinical trials for Overactive Bladder Syndrome

Mirabegron for Female OAB Patients: Comparison of Daytime and Nighttime Dosing

Start date: August 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to elucidate whether night-time dosing of mirebegron can improve nocturia, compared with daytime dosing of mirabegron.

NCT ID: NCT03250650 Completed - Clinical trials for Overactive Bladder Syndrome

Physiotherapy in Overactive Bladder: Electrical Stimulation Treatment

OAB
Start date: March 9, 2017
Phase: N/A
Study type: Interventional

To evaluate the efficacy of combined transvaginal electrical stimulation (ES) and transcutaneous tibial nerve electrical stimulation (TTNS) in the treatment of female overactive bladder syndrome (OAB).

NCT ID: NCT03250585 Completed - Sickle Cell Disease Clinical Trials

sPLA2 in EBC During Acute Chest Syndrome

Start date: January 19, 2018
Phase:
Study type: Observational

Secretory phosholipases A2 (sPLA2) are significantly elevated in the plasma of sickle cell disease patients with acute chest syndrome (ACS), and similar enzymes have been measured in exhaled breath condensate (EBC), which is collected easily and non-invasively. The investigators hypothesize that sPLA2 will be measurable in EBC samples from sickle cell patients with acute chest syndrome.

NCT ID: NCT03249779 Completed - Clinical trials for Restless Legs Syndrome

Treatment of RLS/WED Symptoms Through Sensory Counter-stimulation

RLS/WED
Start date: December 2016
Phase: N/A
Study type: Interventional

To evaluate, in a pilot fashion, efficacy and tolerability of electrical counter-stimulation using the Scrambler device in alleviating uncomfortable sensations and urge to move in patients with restless legs syndrome/Willis Ekbom Disease (RLS/WED).

NCT ID: NCT03247686 Completed - Sjogren's Syndrome Clinical Trials

A Study of RSLV-132 in Subjects With Primary Sjogren's Syndrome

RSLV-132
Start date: February 1, 2017
Phase: Phase 2
Study type: Interventional

The present study will examine the role of circulating RNA complexed with autoantibodies and immune complexes and its role in activation of inflammatory pathways in patients with primary Sjogren's syndrome. The study will be conducted in a subset of Sjogren's patients who have elevated levels of autoantibodies and a pattern of elevated interferon-stimulated gene expression in blood cells. A number of biochemical and clinical parameters will be analyzed to determine the potential therapeutic utility of nuclease therapy in Sjogren's syndrome.