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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00589459
Other study ID # 12258
Secondary ID AHADonaghue Wome
Status Completed
Phase
First received
Last updated
Start date October 1, 2001
Est. completion date December 1, 2008

Study information

Verified date August 2023
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary goal of this study is to measure the prevalence of undiagnosed pre-diabetes/diabetes among women hospitalized with acute coronary syndromes (ACS) compared to men. Inpatients with confirmed ACS (and no known prior history of diabetes) are invited to return to the Yale Hospital Research Unit 6-8 weeks after hospital discharge for an oral glucose tolerance test to identify individuals with pre-diabetes and diabetes.


Recruitment information / eligibility

Status Completed
Enrollment 103
Est. completion date December 1, 2008
Est. primary completion date September 1, 2005
Accepts healthy volunteers No
Gender All
Age group 30 Years and older
Eligibility Inclusion Criteria: - acute coronary syndrome - age > 30 yrs Exclusion Criteria: - previously diagnosed diabetes - ACS due to substance abuse or trauma

Study Design


Locations

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

Sponsors (3)

Lead Sponsor Collaborator
Yale University American Heart Association, Ethel F Donaghue Women's Health Investigator's Program at Yale

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of undiagnosed pre-diabetes or undiagnosed diabetes after hospitalization for acute coronary syndrome
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