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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00675740
Other study ID # Leipzig 03
Secondary ID
Status Completed
Phase Phase 4
First received May 7, 2008
Last updated February 1, 2010
Start date January 2004
Est. completion date February 2007

Study information

Verified date January 2010
Source University of Leipzig
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Interventional

Clinical Trial Summary

The aim of this study is to prospectively assess the relative benefits of either treatment with rosiglitazone or physical exercise on endothelial function in patients with impaired fasting glucose or impaired glucose tolerance and coronary artery disease (CAD).


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date February 2007
Est. primary completion date February 2007
Accepts healthy volunteers No
Gender Both
Age group 35 Years to 70 Years
Eligibility Inclusion Criteria:

- impaired fasting glucose or impaired glucose tolerance

- angiographic evidence of coronary artery disease

Exclusion Criteria:

- diabetes mellitus type I or II

- preexisting antidiabetic medication

- unstable angina

- indication for coronary bypass surgery

- significant left main disease

- myocardial infarction within preceding 3 months

- ejection fraction < 40%

- significant heart valve disease

- severe metabolic disorders

- severe disorders in lipoprotein metabolism

- thyroid disorders

- alcohol or drug abuse

- pregnancy

- participation in another trial

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
rosiglitazone
tablets 4 mg daily
Behavioral:
physical exercise
stationary bike 5-6 times a week
Other:
control
control without intervention

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Leipzig

Outcome

Type Measure Description Time frame Safety issue
Primary between-group difference in flow-mediated dilation of the brachial artery 6 months No
Secondary relative effects of treatment on parameters of - glucose metabolism - inflammatory plasma markers - markers of endothelial function - cellular markers in muscle and fat biopsies 6 months No
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