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Metabolic Syndrome X clinical trials

View clinical trials related to Metabolic Syndrome X.

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NCT ID: NCT00689455 Completed - Metabolic Syndrome Clinical Trials

Regional Observatory on Metabolic Syndrome- LAZIO

ORSA
Start date: October 2007
Phase: N/A
Study type: Observational

The aim of the study, is to assess the prevalence of Metabolic Syndrome in Italy on a regional basis, defined according to NCEP/ATPIII Guidelines criteria.

NCT ID: NCT00687128 Completed - Obesity Clinical Trials

Exercise Dose-Response on Features of the Metabolic Syndrome

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

This study investigates the degree of improvement in insulin resistance and features of the metabolic syndrome in non-diabetic overweight or obese subjects after training in a low-intensity, moderate-intensity or non-aerobic exercise program, as well as self-initiated exercise behavior after the assigned exercise program.

NCT ID: NCT00686244 Completed - Metabolic Syndrome Clinical Trials

IT-Based Training in Metabolic Syndrome

SPRINT
Start date: April 2008
Phase: N/A
Study type: Interventional

Prospective, randomized, single center, controlled intervention study to investigate the effect of a systematic combined personal and IT-based training on the outcome of patients with metabolic syndrome.

NCT ID: NCT00676845 Completed - Hypertension Clinical Trials

Study to Determine if Olmesartan Medoxomil Has the Potential to Benefit the Cardiovascular System in Terms of Arterial Protection

ArtStiff
Start date: August 2008
Phase: Phase 3
Study type: Interventional

This study will analyse the dose-dependent effect of olmesartan medoxomil on the change in arterial stiffness in subjects with hypertension and metabolic syndrome

NCT ID: NCT00675857 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Phase IIa Proof-of-concept Study of NC-503 in Patients With Type II Diabetes

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

The main objectives of the current study are to establish the safety and clinical proof-of-concept of NC-503 in inadequately controlled patients with Type 2 diabetes and features of metabolic syndrome treated with either metformin, a sulfonylurea agent, or metformin in combination with a sulfonylurea agent.

NCT ID: NCT00673023 Completed - Metabolic Syndrome Clinical Trials

Study the Role of Genetic Variation in the Determining Lipid Profile Response to Dietary Change

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

The purpose of this study is to determine whether plasma lipoproteins and lipid responsiveness to a dietary modification is influenced by CETP gene polymorphism.

NCT ID: NCT00671515 Completed - Clinical trials for Depressive Disorder, Major

Pioglitazone for the Treatment of Major Depressive Disorder Comorbid With Metabolic Syndrome

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

The goal of this study is to begin to test whether or not pioglitazone, an FDA approved medication used to treat high blood sugar, may be safe and effective in treating Major Depressive Disorder (MDD) in patients with comorbid Metabolic Syndrome (METSYN).

NCT ID: NCT00666848 Completed - Hypertension Clinical Trials

Effect of Sitagliptin and an ACE Inhibitor on Blood Pressure in Metabolic Syndrome

Start date: March 2008
Phase: Phase 4
Study type: Interventional

This study will measure the effect of the anti-diabetic agent sitagliptin on blood pressure in individuals with the metabolic syndrome. We will also measure the effect of sitagliptin on blood pressure in people already taking a blood pressure medication called an ACE inhibitor.

NCT ID: NCT00666029 Completed - Metabolic Syndrome Clinical Trials

Implications for Treatment of the Metabolic Syndrome

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

To characterize features of metabolic syndrome in volunteers. To undertake a randomised trial to determine whether treatment with a statin improves muscle microvascular blood flow.

NCT ID: NCT00665444 Terminated - Metabolic Syndrome Clinical Trials

Study of Aripiprazole to Reduce Medical Risks in Bipolar Disorder

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

The proposed study is a non-randomized, open label trial that will examine the potential to reduce metabolic risk factors in patients with bipolar I disorder and improve psychiatric and functional outcomes. To accomplish our objective, we plan to conduct a 5-month intervention of 50 obese or overweight adults diagnosed with bipolar disorder. The study will be divided in three steps: Screening, Baseline Period (cross taper to aripiprazole, up to 2 months in duration), Months 1-3 (continued aripiprazole treatment). Subjects will be assessed and meet with their study psychiatrist at least bi-monthly throughout their participation, more frequently when clinically necessary (e.g. during medication tapering or if manic/depressive symptoms emerge). Brief clinical assessments will be conducted at each visit. More thorough assessments will be conducted at Baseline, Week 2, and Month 3.