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Effect of Rosiglitazone in Nondiabetic Patients With the Metabolic Syndrome
This study is ongoing, but not recruiting participants.
Sponsored by: University of Colorado at Denver and Health Sciences Center
Information provided by: University of Colorado at Denver and Health Sciences Center
ClinicalTrials.gov Identifier: NCT00364221
  Purpose

The metabolic syndrome is a collection of health risks that includes obesity, high blood pressure, high triglycerides, high blood sugar, low good cholesterol, and resistance to insulin. The purpose of this study is to find out if the medication, rosiglitazone, influences levels of fat cell proteins and alters insulin resistance in nondiabetic persons with the metabolic syndrome. This is an early step to see if a medication, such as rosiglitazone, will be beneficial in people who have the metabolic syndrome.


Condition Intervention Phase
Metabolic Syndrome
Insulin Resistance
Drug: Rosiglitazone
Phase IV

Drug Information available for: Rosiglitazone Rosiglitazone Maleate
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: The Effect of Rosiglitazone on Adipocyte-Derived Cytokines in Nondiabetics With the Metabolic Syndrome
  Eligibility

Ages Eligible for Study:   30 Years to 55 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Nondiabetic subjects with an NCEP/ATP III diagnosis of the metabolic syndrome

Exclusion Criteria:

  • Statin Medications, liver disease, cardiovascular disease, heart failure, diabetes, chronic kidney disease,
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00364221

Locations
United States, Colorado
University of Colorado at Denver and Health Sciences Center General Clinical Research Center
Denver, Colorado, United States, 80262
Sponsors and Collaborators
University of Colorado at Denver and Health Sciences Center
Investigators
Principal Investigator: Christina L Aquilante, PharmD University of Colorado at Denver and Health Sciences Center
  More Information

Study ID Numbers: COMIRB 04-0447
Study First Received: August 14, 2006
Last Updated: October 4, 2006
ClinicalTrials.gov Identifier: NCT00364221  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Hyperinsulinism
Metabolic Diseases
Insulin Resistance
Metabolic disorder
Glucose Metabolism Disorders
Rosiglitazone

Additional relevant MeSH terms:
Hypoglycemic Agents
Pathologic Processes
Disease
Syndrome
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009