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Syndrome clinical trials

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NCT ID: NCT00682942 Completed - Clinical trials for Acute Respiratory Distress Syndrome

How to Predict Lung Recruitment at the Bedside in Patients Affected by Acute Lung Injury/Acute Respiratory Distress Syndrome (ALI/ARDS)

Start date: May 2008
Phase: N/A
Study type: Observational

The investigators aim to compare four different lung recruitment techniques (described in literature) to Computed tomography scan analysis.

NCT ID: NCT00682890 Terminated - Clinical trials for Polycystic Ovary Syndrome

Combination Metformin and Oral Contraception for Polycystic Ovary Syndrome (PCOS)

Start date: November 2005
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to determine if adding Metformin, a drug that reduces insulin resistance, to birth control pills will reduce the risk of developing type 2 diabetes, high blood pressure. high lipid levels and heart disease in women with PCOS

NCT ID: NCT00682500 Terminated - Clinical trials for Respiratory Distress Syndrome, Adult

Calfactant for Direct Acute Respiratory Distress Syndrome

CARDS
Start date: May 2008
Phase: Phase 3
Study type: Interventional

This study will determine if administration of an suspension of calfactant, a lung surfactant, intratracheally in patients with Direct Acute Respiratory Distress Syndrome within 48 hours of requiring mechanical ventilation can decrease the mortality in patients with lethal disease and shorten the course of respiratory failure in patients with sub-lethal disease.

NCT ID: NCT00682084 Terminated - Insulin Resistance Clinical Trials

Insulin Sensitivity and Substrate Metabolism in Patients With Cushing's Syndrome

Start date: April 2008
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the effect og chronic elevated levels of cortisol on metabolism and insulin sensitivity.

NCT ID: NCT00681863 Terminated - Tourette Syndrome Clinical Trials

Open-label Extension Study of Pramipexole in the Treatment of Children and Adolescents With Tourette Syndrome

Start date: May 2008
Phase: Phase 3
Study type: Interventional

The primary objective of this open-label, flexible dose study is to assess the safety and efficacy of pramipexole over a 24-week period in children and adolescents (age 6-17 years inclusive) diagnosed with Tourette Syndrome according to Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) criteria and who have completed either Study 248.641 (NCT 00681863) or 248.644 (NCT 00558467).

NCT ID: NCT00681616 Recruiting - Clinical trials for Compartment Syndrome

Study of New Catheter & Pressure Monitor System to Help Prevent Compartment Syndrome From Developing in the Injured Leg

TS2
Start date: January 2009
Phase: N/A
Study type: Interventional

An investigation of a new catheter and pressure monitor system that may help to prevent a complication called compartment syndrome from developing in an injured leg. Compartment syndrome occurs when too much fluid builds up in the muscles of the injured leg. This causes a lot of swelling and increases pressures within the leg that can cause permanent damage muscles and nerves in the leg.

NCT ID: NCT00680693 Completed - Clinical trials for Irritable Bowel Syndrome

Mindfulness vs. Support Groups for Irritable Bowel Syndrome

M-IBS
Start date: October 2006
Phase: N/A
Study type: Interventional

Irritable bowel syndrome (IBS) is a common and disabling functional disorder characterized by significant abdominal discomfort and disturbed defecation. It affects over 10% of U.S. adults (14% women, 8% men), resulting in major disability, impaired quality of life, and a significant health-care burden. Conventional management of IBS is only partially effective in some patients and includes use of medications, behavioral modification, dietary approaches, and lifestyle changes such as exercise and stress reduction. Although behavioral treatments such as cognitive behavioral therapy and hypnosis have been among the most effective treatments, they are costly to deliver. Mindfulness meditation, a complementary/alternative medicine (CAM) therapy taught in groups, is a unique self-regulatory, mind-body approach in which practitioners learn to attend to present-moment experiences, letting go of fixation on negative emotions and thoughts of past and future. It has been found to be effective in reducing chronic pain and stress and in ameliorating disorders with similarities to IBS, including fibromyalgia, headache, and depression. The overall goals of this exploratory, pilot study of women with IBS are to compare mindfulness meditation training to a patient support group (a previously validated control condition) in a small, randomized controlled clinical trial, in order to assess the feasibility of a larger, definitive trial. Specific aims are to evaluate primary and secondary outcome measures, to assess expectancy of benefit and scales measuring mindfulness (process measures), and to identify barriers to conducting such a trial in our setting. Sixty women meeting Rome II diagnostic criteria for IBS will be randomly assigned to one of two treatments - mindfulness meditation training or a support group - and will undergo 8 weekly group sessions plus a single day-long session. The primary outcome measure is improvement on the validated Irritable Bowel Symptom Severity Scale from pretreatment to the end of treatment, with follow-up at 3, 6, and 12 months. Additional variables address alternative endpoints (e.g., Adequate Relief of IBS symptoms, disease specific quality of life) and mechanism of treatment effects (e.g., coping scales, psychological symptoms, Visceral Sensitivity Scale). The multidisciplinary research team includes physicians, psychologists, and educators.

NCT ID: NCT00679679 Completed - Clinical trials for Polycystic Ovary Syndrome

Metformin and Lifestyle Intervention in Women With Polycystic Ovary Syndrome

Start date: January 2003
Phase: Phase 4
Study type: Interventional

Polycystic ovary syndrome is a frequent cause of abnormal menses and infertility. It has also been related to cardiovascular disease. The objective of this trial is to evaluate the clinical and metabolic efficacy of metformin plus life style modifications in women with polycystic ovary syndrome compared with life style modifications and placebo

NCT ID: NCT00677976 Completed - Clinical trials for Irritable Bowel Syndrome

Use of Functional Magnetic Resonance Imaging (fMRI) to Study Brain Activation in Children With Irritable Bowel Syndrome

fMRI
Start date: June 2007
Phase:
Study type: Observational

The purpose of the study is to map regions of brain activation following rectal stimulation in children with irritable bowel syndrome (IBS) and healthy controls.

NCT ID: NCT00677053 Completed - Clinical trials for Acute Coronary Syndrome

Safety and Efficacy of TAK-442 in Subjects With Acute Coronary Syndromes

Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of multiple doses of TAK-442once daily, (QD) or twice daily (BID), in subjects with acute coronary syndrome (unstable angina, myocardial infarction).