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NCT00589355 Clinical Trial

C-reactive Protein and Endothelial Dysfunction in Women With Glucose Intolerance

Glucose Intolerance Clinical Trial

Official title:
C-reactive Protein and Endothelial Dysfunction in Women With Glucose Intolerance

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00589355
Other study ID # 12110
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2002
Est. completion date October 1, 2008

Study information
Verified date April 2020
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study is to determine whether markers of vascular inflammation (such as c-reactive protein) can predict endothelial dysfunction (as measured by flow-mediated dilation) in postmenopausal women with glucose intolerance compared to normal controls.

Recruitment information / eligibility
Status Completed
Enrollment 46
Est. completion date October 1, 2008
Est. primary completion date June 2003
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria:

- healthy postmenopausal women

- ages 40-65

Exclusion Criteria:

- smokers

- diabetes requiring medication

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Yale Center for Clinical Investigation New Haven Connecticut

Sponsors (1)
Lead Sponsor Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary c-reactive protein performed after screening evaluation
Secondary flow-mediated dilation of brachial artery performed twice after screening visit
Secondary sex steroids performed after screening visit
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