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Syndrome clinical trials

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NCT ID: NCT00639730 Completed - Epilepsy Clinical Trials

Use of the Atkins Diet for Children With Sturge Weber Syndrome

Start date: May 2006
Phase: Phase 1
Study type: Interventional

This research is being done to find out if the Atkins Diet can be used safely and effectively to reduce seizures in children who have Sturge Weber syndrome. The ketogenic diet is a proven therapy for epilepsy, but can be difficult to use in children. The Atkins Diet is a high fat, high protein, low carbohydrate diet introduced in the 1970s to help with weight loss. It is different from the ketogenic diet in four major ways: no calorie restriction, no fluid restriction, no protein restriction, and is easy to start outside the hospital. People on the Atkins Diet become ketotic (produce high levels of ketones, a certain substance in the body), like patients on the ketogenic diet, and the investigators believe this may lead to seizure control. Children aged 2-18 with Sturge Weber syndrome and seizures at least monthly, who have used at least two anti-seizure drugs may join. 5 children in total will be enrolled.

NCT ID: NCT00638547 Completed - Hurler Syndrome Clinical Trials

Intrathecal Enzyme Replacement for Hurler Syndrome

Start date: January 2, 2008
Phase: Phase 1
Study type: Interventional

This protocol will examine whether the enzyme alpha-L-iduronidase (Laronidase), delivered into the spinal fluid of patients with Hurler syndrome at intervals before and after bone marrow transplant, is a safe and effective approach to slow the neurologic degeneration seen in Hurler patients undergoing transplantation.

NCT ID: NCT00637793 Completed - Sjogren's Syndrome Clinical Trials

Study of NGX267 Oral Capsules in Patients With Xerostomia Associated With Sjorgren's Syndrome

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

The purpose of this study is to evaluate the effectiveness of NGX267 in the improvement of decreased salivary flow associated with primary or secondary Sjögren's syndrome. For each patient, the study includes four periods of treatment separated by a washout period that may range from 4 - 8 days according to patient and site discretion. Each treatment period includes two overnight stays in the clinic. One dose of study drug is taken during each treatment period

NCT ID: NCT00637572 Completed - HIV Infections Clinical Trials

Evaluate Weight Gain Using 2 Different Formulations of Megestrol Acetate Oral Suspension for AIDS-related Weight Loss

Start date: December 2004
Phase: Phase 2
Study type: Interventional

Explore weight gain in HIV-positive patients who have weight loss associated with AIDS-related wasting (anorexia/cachexia). Patients are treated for 12 weeks with either megestrol acetate oral suspension nanocrystal dispersion formulation, or megestrol acetate oral suspension original formulation

NCT ID: NCT00637507 Completed - Clinical trials for Respiratory Distress Syndrome

Study of a Novel Technique of Mechanical Ventilation in Patients With Severe Acute Respiratory Failure

HFO-TGI-2
Start date: March 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators have recently demonstrated the beneficial effects of combined high-frequency oscillation (HFO) and tracheal gas insufflation (TGI) on the respiratory physiology [1,2] of patients with severe acute respiratory distress syndrome (ARDS) (NCT00416260). Preliminary short-term survival results were also encouraging. Consequently, in the present clinical trial, the investigators intend to increase the size of the studied population, in order to evaluate the effect of HFO-TGI on survival with adequate statistical power. Furthermore, the investigators intend to elucidate the mechanism of the HFO-TGI-related physiological benefit.

NCT ID: NCT00637221 Completed - Fragile X Syndrome Clinical Trials

Open Label Study Investigating Safety and Efficacy of NPL2009 50 mg - 150 mg on Prepulse Inhibition Tests and Continuous Performance Tasks, Adults With Fragile X Syndrome

Start date: March 2008
Phase: Phase 1/Phase 2
Study type: Interventional

This is an open label exploratory study to investigate the safety and effects of a single dose of NPL-2009(50 mg - 150 mg) on Prepulse Inhibition (PPI) Tests and Continuous Performance Tasks (CPT) in adults with Fragile X Syndrome

NCT ID: NCT00636649 Completed - Clinical trials for Night Eating Syndrome

Escitalopram Treatment of Night Eating Syndrome

Start date: October 2008
Phase: N/A
Study type: Interventional

Night-Eating Syndrome (NES) is an eating disorder characterised by excessive eating at night, sleep disturbance and morning anorexia. This 12-week study examines the effect of escitalopram on symptoms of NES.

NCT ID: NCT00635674 Completed - Metabolic Syndrome Clinical Trials

Effects of CPAP on Cardiovascular Risk in Obstructive Sleep Apnea (OSA) and Metabolic Syndrome

Start date: February 2007
Phase: N/A
Study type: Interventional

The increased risk of atherosclerotic morbidity and mortality in patients with obstructive sleep apnea (OSA) has been linked to arterial hypertension, insulin resistance, systemic inflammation, and oxidative stress in previous studies. We aimed to determine the effects of 8-weeks therapy with continuous positive airway pressure (CPAP) on glucose and lipid profile, systemic inflammation, oxidative stress, and the global cardiovascular disease (CVD) risk in patients with severe OSA and metabolic syndrome.

NCT ID: NCT00634699 Completed - Clinical trials for Carpal Tunnel Syndrome

The Treatment of Carpal Tunnel Syndrome Using Thumb Pressure Along the Median Nerve

Start date: September 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find the efficacy of treating the muscles in the inside (biceps,pronator teres) of the arm in order to eliminate the carpal tunnel syndrome .The authors hypothesise that eliminating the trigger points located in these muscles would diminish the symptoms associated with the carpal tunnel syndrome.

NCT ID: NCT00633971 Completed - Clinical trials for Post Thrombotic Syndrome

Treatment Trial for Post-Thrombotic Syndrome

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if complex lymphedema therapy is effective in decreasing disease severity and improving quality of life in patients with post thrombotic syndrome.