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Syndrome clinical trials

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NCT ID: NCT00829439 Completed - Angelman Syndrome Clinical Trials

Study on Tolerability of Levodopa/Carbidopa in Children With Angelman Syndrome

Start date: January 2009
Phase: Phase 1
Study type: Interventional

This study is designed to determine the highest dose of levodopa/carbidopa that can be tolerated without any serious side effects by children with Angelman syndrome. It has been hypothesized that levodopa may lead to an improvement in the neurodevelopment and abnormal movements (e.g. tremors) in children with Angelman syndrome. Data from this study will be used to design a phase II trial to determine the efficacy of levodopa in treating children with Angelman syndrome.

NCT ID: NCT00829218 Completed - Fibromyalgia Clinical Trials

Clinical Trial Examining Effects of Monosodium Glutamate (MSG) on Irritable Bowel Syndrome (IBS) and Fibromyalgia (FM)

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

Objective: Randomized, double blind, placebo-controlled, crossover, clinical trial to examine the effects of the food additive glutamate (in the form of MSG) on IBS and fibromyalgia. Setting and Subjects: The Fibromyalgia Research Database at OHSU will be utilized to identify and recruit fibromyalgia patients who also have IBS to OHSU study centers. Intervention: Approximately 60 male and female subjects aged 18-75 will be placed on a 1-month glutamate-free elimination diet. Those that respond positively to the diet (we are estimating 30-40 subjects), will then be randomized to receive either a citrus drink containing 5 grams of MSG; or placebo (the citrus drink alone)on three consecutive days one week apart. The investigators are hypothesizing that those who react positively to the elimination diet will have symptom occurrence statistically more frequently when given the glutamate challenge, than when given placebo.

NCT ID: NCT00828802 Completed - Clinical trials for Myelodysplastic Syndromes

Lenalidomide and Decitabine in High Grade Myelodysplastic Syndromes

Start date: March 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out what dose of lenalidomide is safe to use in combination with decitabine when given in people with myelodysplastic syndrome.

NCT ID: NCT00825617 Completed - Turner Syndrome Clinical Trials

Quantitative Liver Functions in Turner Syndrome With and Without Hormone Replacement Therapy

Start date: October 1996
Phase: N/A
Study type: Interventional

Several studies have demonstrated that Turner Syndrome patients have elevated liver enzymes readily suppressible by a short course of HRT. We wanted to estimated quantitative liver functions in a young group of Turner syndrome patients compared to a healthy control group.

NCT ID: NCT00825175 Completed - Down Syndrome Clinical Trials

Treadmill Training and Orthotic Use in Infants With Down Syndrome

Start date: March 2006
Phase: N/A
Study type: Interventional

This study determines the effect of orthotic use in combination with treadmill training on the development of gross motor skills and walking onset in infants with Down syndrome.

NCT ID: NCT00824395 Withdrawn - Type 2 Diabetes Clinical Trials

The Genetics of Diabetes in Southern California Chinese Americans

Start date: January 2006
Phase:
Study type: Observational

The purpose of this research study is to investigate the genetic causes of diabetes. Specifically, we are interested in the mitochondrial genome and how variants in the mitochondrial genome influence a person's risk to develop diabetes and metabolic syndrome.

NCT ID: NCT00824122 Completed - Red Man Syndrome Clinical Trials

Vancomycin Associated Red Man Syndrome (RMS)

Start date: January 2008
Phase: Phase 4
Study type: Observational

This study proposes to identify patients who developed RMS with vancomycin infusion, and determine presence or absence of variant alleles involved in histamine biotransformation. The implications of this study are important, as identification of variant alleles in these patients, may alter the current standard of care for vancomycin infusions. The hypothesis of this study is that the development of red man syndrome (RMS) during receipt of intravenous vancomycin is associated with the presence of variant alleles for genes involved in the histamine pathway. The primary outcome that will be measured will be the history of RMS and the presence or absence of variant alleles for the genes responsible for histamine metabolism (i.e. histamine n-methyltransferase and diamine oxidase). As a secondary endpoint, the study will also attempt to determine the incidence of RMS in pediatric patients.

NCT ID: NCT00822679 Recruiting - Clinical trials for Acute Coronary Syndrome

Eszopiclone and Inflammatory Mediators in Patients With Acute Coronary Syndrome

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of the study is to examine the effects of Eszopiclone, a sleep aid, on inflammatory mediators and coagulability in patients with a recent myocardial infarction.

NCT ID: NCT00822107 Completed - Gitelman Syndrome Clinical Trials

A Translational Approach to Gitelman Syndrome

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

This study will test the response to a single dose of thiazide diuretic as a diagnostic test for Gitelman syndrome. Individuals with hypokalemic alkalosis will be enrolled. After a baseline study, they will have the response to 50 mg hydrochlorothiazide on fractional chloride excretion examined.

NCT ID: NCT00821314 Recruiting - Clinical trials for Overactive Bladder Syndrome

The Effect of Position on Urge Sensation in Volunteers and in Patients With Overactive Bladder Syndrome

Start date: April 2009
Phase: N/A
Study type: Observational

Importance of the problem OAB is a common health problem. Milsom et al. [1] randomly selected a population from six European countries. From this population, 17% of the respondents reported having OAB symptoms with 14% reporting frequency, 9% urgency, and 6% urge incontinence. The study by Milsom et al. [1] showed that OAB adversely affected the lives of the majority (65%) of the respondents who reported OAB symptoms. Chen et al. [2] also reported that the prevalence of OAB in Taiwanese women was similar to that of Western women. In the study of Chen et al.[2], the prevalence of OAB was 18.6% for the patients; perceptions and the number of OAB condition significantly increased in the elderly women (over 65 years old, 39.3%). Apart from impairing the physical health, OAB may have a tremendous effect on psychological and social well-being. Information on the symptoms and disease severity can yield important information that often complements objective measures. Incontinence, increased urge and increased frequency of micturition affect nearly 100 million people in the western world (33 million in the US and 66 million in the European Union). These conditions are not life threatening but they seriously affect quality of life and ability to work. OAB is in some studies reported to have an incidence of up to 17 % in the western population with great consequences for the quality of life. Economic cost The total economic cost of this group of conditions is high. In 2002 the costs in the US were approximately $12.7 billion[1] (estimated to be $17 billion and €22 billion/year in 2005). Approximately 25% of this expenditure is spent on treatment (drug therapy, clinical consultation and surgery). Of those who suffer only 28% have sought help and only half of those currently receive treatment. Less than 3% regain long lasting normal control. Therefore, these costs are an under-estimate and the problem is large. Aetiology