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OpenTrials
Completed

NCT Number: NCT00589459

Gender Differences in Prevalence of Undiagnosed Diabetes in ACS

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.

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Key information

Age range

30 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Bridgeport Hospital, Bridgeport, Connecticut, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • acute coronary syndrome
  • age > 30 yrs

Exclusion criteria

  • previously diagnosed diabetes
  • ACS due to substance abuse or trauma

Treatment and study plan

Primary outcomes

  1. Prevalence of undiagnosed pre-diabetes or undiagnosed diabetes

    Time frame: after hospitalization for acute coronary syndrome

Sponsors and collaborators

Lead sponsor

Yale University

Other

Collaborators

  • American Heart Association
  • Ethel F Donaghue Women's Health Investigator's Program at Yale

Registry information

Official study title

A Pilot Study of Gender Differences in the Prevalence of Undiagnosed Diabetes in Acute Coronary Syndromes (ACS)

Important dates

Study start
2001
Primary completion
2005
Study completion
2008
First posted
Jan 9, 2008
Registry last updated
Aug 30, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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