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Syndrome clinical trials

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NCT ID: NCT00413400 Completed - Metabolic Syndrome Clinical Trials

Study of TNF-Antagonism in the Metabolic Syndrome (II)

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

This study will investigate whether etanercept will result in improved inflammatory indices, glucose tolerance and endothelial function in patients with the metabolic syndrome.

NCT ID: NCT00413114 Completed - Clinical trials for Myelodysplastic Syndromes

Safety and Efficacy of Obatoclax Mesylate (GX15-070MS)for the Treatment of Myelodysplastic Syndromes (MDS)

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

Defects in the apoptotic process can lead to the onset of cancer by allowing cells to grow unchecked when an oncogeneic signal is present. Obatoclax is designed to restore apoptosis through inhibition of the Bcl-2 family of proteins, thereby reinstating the natural process of cell death that is often inhibited in cancer cells. This is a multi-center, open-label, Phase II study of obatoclax administered in 2-week cycles to patients with previously-untreated Myelodysplastic Syndromes with anemia and/or thrombocytopenia. Treatment may be administered on an outpatient basis. No investigational or commercial agents or therapies other than those described herein may be administered with the intent to treat the patient's malignancy. Supportive care measures including those directed at controlling symptoms resulting from Myelodysplastic Syndromes are allowed

NCT ID: NCT00412802 Completed - Clinical trials for Acute Coronary Syndrome

Adaptation Dose of Enoxaparin in Moderate Renal Failure Patients With Acute Coronary Syndrome

Start date: December 2006
Phase: Phase 4
Study type: Interventional

The objective of the VALIDE study is to validate that a 25% dose reduction of enoxaparine in patients with moderate renal failure (creatinine clearance between 30 and 50 ml/min) and hospitalized for an acute coronary syndrome provides at steady state a similar anti Xa level in plasma compared to that obtained in patients without renal failure and receiving the usual dose of 1 mg/kg subcutaneously every 12 hours. 140 per - protocol patients are planned to be included.

NCT ID: NCT00411905 Recruiting - Clinical trials for Myelodysplastic Syndromes

Bortezomib and Low Dose Cytarabine in the Treatment of High-Risk Myelodysplastic Syndromes

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

We are evaluating the efficacy of the association of Low dose Cytarabine in association with Bortezomib in the treatment of patients diagnosed with high risk Myelodysplastic syndromes. Our aim is to decrease transfusion requirements and if possible induce a complete or at least a partial remission.

NCT ID: NCT00409773 Completed - Metabolic Syndrome Clinical Trials

Ezetimibe/Simvastatin in Patients With Metabolic Syndrome (0653A-107)(COMPLETED)

Start date: January 2007
Phase: Phase 3
Study type: Interventional

A 6-week clinical trial in patients with metabolic syndrome and hypercholesterolemia at high risk for coronary heart disease to study the effects of ezetimibe/simvastatin and atorvastatin on lipids.

NCT ID: NCT00409578 Completed - Myocardial Ischemia Clinical Trials

Efficacy and Safety of Aliskiren and Valsartan Versus Placebo in Patients Stabilized Following an Acute Coronary Syndrome

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

The purpose of this study is to test the hypothesis that the inhibition of the renin-angiotensin-aldosterone system (RAAS) with the angiotensin receptor blocker valsartan or the renin antagonist aliskiren will improve ventricular hemodynamics, as reflected by a greater reduction in levels of N-terminal proB-type natriuretic peptide (NT-proBNP) compared to placebo in subjects stabilized following acute coronary syndrome (ACS) who are determined to be at high risk due to an elevated concentration of natriuretic peptides.

NCT ID: NCT00409539 Completed - Clinical trials for Overactive Bladder Syndrome (OABS)

SMP-986 Phase 2 Proof of Concept in Patients With Overactive Bladder Syndrome (OABS)

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

SMP-986 is a compound being developed for the treatment of overactive bladder syndrome (OABS). This clinical study is designed to test the hypothesis that SMP-986 at doses of 20mg, 40mg, 80mg or 120mg provides greater symptom relief in OABS compared to placebo. The hypothesis will be tested by measuring the change in mean voids/24 hrs after treatment with SMP-986 compared to placebo, as well comparing the change in: the severity of urgency episodes, mean number of urgency episodes/24 hr, mean number of incontinence episodes/24 hr and the mean void volume/void between SMP-986 and placebo.

NCT ID: NCT00409435 Recruiting - Clinical trials for Postural Tachycardia Syndrome

A Study of Pyridostigmine in Postural Tachycardia Syndrome

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

This is a 3-day study comparing pyridostigmine versus placebo in the treatment of postural tachycardia syndrome (POTS). The researchers expect pyridostigmine to improve tachycardia and stabilize blood pressure.

NCT ID: NCT00409318 Completed - Metabolic Syndrome Clinical Trials

Study of TNF-Antagonism in Metabolic Syndrome

Start date: April 2004
Phase: N/A
Study type: Interventional

This study investigates whether blockade of TNF will result in reduced inflammatory indices in patients with the metabolic syndrome

NCT ID: NCT00408850 Recruiting - Metabolic Syndrome Clinical Trials

Effects of Pioglitazone Treatment on Sympathetic Nervous System Function in Metabolic Syndrome Obesity

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

An abdominal distribution of fat is associated with the greatest heart disease risk, because commonly, several risk factors of metabolic origin cluster in these individuals. When this occurs the condition is called the 'metabolic syndrome'. Increased activity of the sympathetic nervous system resulting in enhanced release of the stress hormone 'noradrenaline', may be one mechanism by which adverse cardiovascular and metabolic sequela of the metabolic syndrome might be mediated. Impaired insulin action may be one factor contributing to increased noradrenaline release. The aim of this Study is to determine whether treatment with a drug called pioglitazone which is known to improve insulin action, results in reduced sympathetic nervous system activity and stress hormone release when compared to treatment with a dummy drug (placebo).