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Syndrome clinical trials

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NCT ID: NCT00444964 Completed - Clinical trials for Prader-Willi Syndrome

Growth Hormone Use in Adults With Prader-Willi Syndrome

Start date: April 2005
Phase: Phase 3
Study type: Interventional

The main research question this protocol aims to answer is whether treatment with growth hormone will impact body composition, quality of life, and energy balance in PWS adults, and if there is a loss of effects after cessation of treatment for at least 12 months.

NCT ID: NCT00444886 Completed - Clinical trials for Thoracic Outlet Syndrome

Treatment of Thoracic Outlet Syndrome (TOS) With Botox

Start date: May 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is: 1. To assess the effect of BOTOX injection to the scalene muscles on the severity of pain from TOS. 2. To assess the effect of BOTOX injection on numbness and tingling and quality of life.

NCT ID: NCT00444717 Completed - Metabolic Syndrome Clinical Trials

Impact of Pitavastatin in Hypercholesterolemic Patients With Metabolic Syndrome

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

The purpose of this study is to evaluate anti-oxidative and anti-inflammatory effects of pitavastatin in hypercholesterolemic patients with the metabolic syndrome.

NCT ID: NCT00444288 Completed - Clinical trials for Polycystic Ovary Syndrome

PCOS Twin Study - Environmental Factors in the Development of Polycystic Ovary Syndrome, Phase 2

Start date: February 27, 2007
Phase: N/A
Study type: Observational

Polycystic Ovary Syndrome, or PCOS, is the most common endocrine disorder in women. Depending on the strictness of the diagnostic criteria used, it is thought to occur in about 6-10% of all women, many of whom do not know they have the syndrome. Women with PCOS produce abnormally high levels of male hormones (hyperandrogenism); this counteracts their ovaries' ability to make enough of the female hormones estrogen and progesterone needed for normal menstruation. PCOS is the number one cause of hormonally related infertility and also increases women's risks for diabetes, high blood pressure, hypercholesteremia, cardiovascular disease and certain cancers. It is currently unclear to what extent PCOS and PCOS-associated traits (hyperandrogenisms, hyperinsulinemia, insulin resistance, type 2 diabetes, dyslipidemia, hypertension, obesity, and coronary artery disease) are the results of environmental factors or genetic predisposition. Therefore, the NIEHS Program in Clinical Research is conducting a multi-phase twin study to measure the extent of PCOS heritability and to identify environmental and genetic factors involved in the development of PCOS. The proposal described here is for Phase 2 of this study. The goals of Phase 2 are to: 1) establish more reliable concordance rates and baseline heritability estimates for PCOS in MZ and DZ twins; and 2) establish a cohort of intact MZ and DZ female twin pairs as a resource for future studies. In Phase 1, about 1500 individual female twins were identified from the Mid-Atlantic Twin Registry (MATR) based on self report of a history of irregular periods and/or cystic ovaries in the MATR General Health Screening Questionnaire. Those twins were surveyed by phone for other traits associated with PCOS. In Phase 2, the twins most likely to have PCOS based on their answers to the Phase 1 phone survey will be recontacted for further PCOS screening. This includes providing a blood sample for measuring bioavailable testosterone (BaT) levels. Women with elevated BaT levels are likely to have PCOS. The women with elevated levels will then be asked to undergo a medical evaluation for PCOS confirmation. This includes a physical exam, medical history, ultrasound, 2-hour glucose tolerance and other biochemical blood tests, and a Ferriman-Gallwey evaluation for abnormal hirsutism (another characteristic of PCOS). The women will also be tested for pregnancy and zygosity. Their female co-twins will be invited to undergo...

NCT ID: NCT00443339 Recruiting - Clinical trials for Myelodysplastic Syndromes

Darbepoetin Alpha in Myelodysplastic Syndromes (MDS)

Start date: December 2006
Phase: Phase 2
Study type: Interventional

This is an evaluation of the effectiveness of darbepoetin alpha in treating anemia of MDS patients with an International Prognostic Scoring System (IPSS) score of low or intermediate 1.

NCT ID: NCT00443144 Completed - Turner Syndrome Clinical Trials

D3-GHR Polymorphism and Turner Syndrome

Start date: May 2005
Phase: N/A
Study type: Observational

The protein polymorphism of the growth hormone receptor characterized by the genomic deletion of exon 3 has been linked to the magnitude of the first-year-growth response to growth hormone (GH) in girls with Turner syndrome. Objective: to study the long-term effect of GH therapy in Turner syndrome in correlation to this GHR polymorphism in a mainly retrospective design (chart-review).

NCT ID: NCT00442949 Completed - Clinical trials for Acute Coronary Syndrome

Angioplasty to Blunt the Rise of Troponin in Acute Coronary Syndrome (ACS)

ABOARD
Start date: August 2006
Phase: N/A
Study type: Interventional

Release of troponin evaluated by the peak of troponin during the hospital phase.Because of its sensitivity and specificity as well as its widespread use in routine practice, rise in troponin levels is the main assessment criteria of this study. We plan to demonstrate a significantly altered distribution of the troponin release as evaluated by the peak of troponin for each patient during the hospitalization period (from randomization to cardiologic unit discharge), in the two arms of the trial.

NCT ID: NCT00442689 Completed - Metabolic Syndrome Clinical Trials

Metabolic Syndrome in PCOS: Precursors and Interventions

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

The purpose of this study is to investigate the metabolic effects of anti-androgens and oral contraceptive pills (OCPs), compared with placebo, in the treatment of women with PCOS. We hypothesized that controlling elevated androgen levels with either anti-androgens or OCPs would produce improvement in metabolic markers in PCOS women and would reduce their long term metabolic risk.

NCT ID: NCT00442273 Completed - Dry Eye Syndrome Clinical Trials

Comparison of Autologous Serum and Umbilical Cord Serum Eyedrops for Dry Eye Syndrome

Start date: n/a
Phase: N/A
Study type: Interventional

To compare the therapeutic effect between autologous serum and umbilical cord serum eyedrops in the treatment of severe dry eye syndrome.

NCT ID: NCT00442182 Recruiting - Clinical trials for Autoinflammatory Syndromes

The Efficacy and Safety of ITF2357 in AIS

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

Autoinflammatory syndromes (AIS) are a group of disorders characterized by recurrent episodes of inflammation.Although for the hereditary autoinflammatory diseases the genetic mutations are known it remains largely unclear how these mutations lead to recurrent inflammatory attacks. Treatment of the inflammatory symptoms remains a challenge. With beneficial responses reported during treatment with simvastatin, etanercept or anakinra in some but not all patients. ITF2357 is an orally active histon deacetylase inhibitor with a potent anti-inflammatory effect due to inhibition of pro-inflammatory cytokines (IL-1β, TNFα, IFNg, IL-6). We expect that ITF2357 is able to modify the clinical symptoms of AIS patients and induce clinical complete remission or a reduction in attack duration.