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Syndrome clinical trials

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NCT ID: NCT00579813 Completed - Metabolic Syndrome Clinical Trials

Mechanisms Underlying Metabolic Syndrome in Obesity

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

The purpose of this study is to better understand the link between obesity and diabetes or pre-diabetes.

NCT ID: NCT00579709 Completed - DiGeorge Syndrome Clinical Trials

Thymus Transplantation With Immunosuppression

884
Start date: July 2002
Phase: Phase 1
Study type: Interventional

The research purpose is to determine if thymus transplantation with immunosuppression is a safe and effective treatment for complete DiGeorge anomaly. The research includes studies to evaluate whether thymus transplantation results in complete DiGeorge anomaly subjects developing a normal immune system.

NCT ID: NCT00579657 Completed - Obesity Clinical Trials

Protein, Fiber, and Metabolic Syndrome - The PROFIMET Study

PROFIMET
Start date: August 2007
Phase: N/A
Study type: Interventional

Randomized controlled single-blinded intervention study in 111 overweight and obese subjects with risk factors of developing type 2 diabetes, with the aim to investigate effects of isoenergetic high cereal fiber as compared with high protein diets over 6 and 18 weeks. Proof of principle study with analysis according to study protocol, investigating whether isoenergetic high cereal fiber and high protein diets with comparable fat contents, if adhered to and after exclusion of known confounders such as changes in body weight, intake of drugs with known effects on insulin sensitivity, or relevant changes in physical activity, indeed affect insulin sensitivity.

NCT ID: NCT00579527 Completed - Clinical trials for Complete DiGeorge Syndrome

Phase I/II Thymus Transplantation With Immunosuppression #950

#950
Start date: December 19, 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The study purpose is to determine if cultured thymus tissue implantation (CTTI) (previously described as transplantation) with tailored immunosuppression based on the recipient's pre-implantation T cell population is a safe and effective treatment for complete DiGeorge anomaly. This study will also evaluate whether cultured thymus tissue implantation and parathyroid transplantation with immunosuppression is a safe and effective treatment for complete DiGeorge anomaly and hypoparathyroidism.

NCT ID: NCT00578825 Not yet recruiting - Clinical trials for Severe Acute Respiratory Syndrome

A Multi-centre, Double-blinded, Randomized, Placebo-controlled Trial on the Efficacy and Safety of Lopinavir / Ritonavir Plus Ribavirin in the Treatment of Severe Acute Respiratory Syndrome

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

The study aims to examine whether the combination of Lopinavir/Ritonavir plus Ribavirin for treatment of severe acute respiratory syndrome (SARS) is superior to placebo.

NCT ID: NCT00576836 Completed - DiGeorge Syndrome Clinical Trials

Thymus Transplantation Dose in DiGeorge #932

Start date: September 2, 2004
Phase: Phase 2
Study type: Interventional

One purpose of this study is to determine whether the amount of cultured thymus tissue implanted into DiGeorge anomaly infants has any effect on the immune outcome. Another purpose of this study is to determine whether parental parathyroid transplantation (in addition to cultured thymus tissue implantation (CTTI) can help both the immune and the calcium problems in DiGeorge infants with hypocalcemia. [Funding Source - FDA Office of Orphan Products Development (OOPD)]

NCT ID: NCT00576407 Completed - DiGeorge Syndrome Clinical Trials

Thymus Transplantation in DiGeorge Syndrome #668

Start date: October 1991
Phase: Phase 2
Study type: Interventional

The study purpose is to determine whether cultured thymus tissue implantation (CTTI) is effective in treating typical complete DiGeorge syndrome.

NCT ID: NCT00575653 Completed - Clinical trials for Guillain-Barre Syndrome

Safety Study of GBS Following Menactra Meningococcal Vaccination

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

We are conducting a large, record-based study to assess the risk of Guillain-Barré Syndrome (GBS), a serious demyelinating disease, following immunization with the tetravalent meningococcal conjugate vaccine (Menactra) that is currently recommended for all adolescents. The study was requested by CDC and FDA because of an unexpected number of case reports to the CDC's Vaccine Adverse Event Reporting System (VAERS). The study protocol was designed by the investigators, with input from FDA, CDC, and the vaccine's manufacturer, Sanofi-Pasteur. An external advisory board that includes CDC representation, provides input regarding important decisions. The manufacturer is not participating in the conduct of the study and has no control over the analysis or dissemination of results. The study is derived from five large US health plans with a total membership of approximately 50 million over the study time period. America's Health Insurance Plans (AHIP) serves as liaison between the health plans and the Coordinating Center at the Department of Ambulatory Care and Prevention of Harvard Medical School and Harvard Pilgrim Health Care, and is the contracting organization with the health plans.

NCT ID: NCT00573950 Unknown status - Clinical trials for Diabetes Mellitus, Type 2

Effects of Cilostazol on Plasma Adipocytokine and Arterial Stiffness

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

Cilostazol is an antiplatelet agent used to reduce the symptoms of intermittent claudication. Cilostazol inhibits phosphodiesterase III (PDE III), which causes it to be a vasodilator and inhibitor of platelet aggregation. Recently there were report of beneficial effect of cilostazol like vasodilation, lipid metabolism, and cytokine production. But there were few clinical studies that support these effects of cilostazol. The purpose of this study is to evaluate the vasodilatory and anti-inflammatory effect of cilostazol presented by PWV and plasma adipocytokines.

NCT ID: NCT00571727 Completed - Clinical trials for Growth Hormone Insensitivity Syndrome

Long-Term Treatment With rhIGF-1 in GHIS

Start date: May 20, 1991
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of this study was to evaluate the long-term safety and effectiveness of mecasermin (the study drug) in children with growth failure due to severe Primary insulin-like growth factor-1 deficiency (Primary IGFD).