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A Phase 4 Study of Stress Heart Imaging in Patients with Diabetes at Risk for Coronary Disease. - Article


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Gestational Diabetes

Diabetes, Gestational


Clinical Trial: A Phase 4 Study of Stress Heart Imaging in Patients with Diabetes at Risk for Coronary Disease.

This study is currently recruiting patients.
Verified by Bristol-Myers Squibb September 2005

Sponsored by: Bristol-Myers Squibb
Information provided by: Bristol-Myers Squibb
ClinicalTrials.gov Identifier: NCT00162344

Purpose

The study is designed to see if stress heart imaging can be used as a screening exam in patients with diabetes and risk factors of developing of coronary artery disease and experiencing future cardiac events.
Condition Intervention Phase
Diabetes
 Drug: Technetium Tc99m Sestamibi
Phase IV

MedlinePlus related topics:  Diabetes

Study Type: Interventional
Study Design: Diagnostic, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study

Official Title: AceP-D: Non-Invasive Assessment of Atypical Chest Pain in Patients with Diabetes

Further Study Details: 
Primary Outcomes: Examine the prevalence of ischemic heart disease in population of patients with diabetes mellitus and atypical chest pain.
Secondary Outcomes: Determine the accuracy of myocardial perfusion imaging (MPI) and exercise tolerance testing (ETT) for the detection of coronary artery disease (CAD) in a subset of patients undergoing clinically indicated coronary angiography.; Determine the relative value of ETT, Duke Treadmill Score (DTS), MPI, ejection fraction (EF), clinical risk factors, and C-Reactive Protein (CRP) values for identifying patients at risk for cardiac events.
Expected Total Enrollment:  500

Study start: December 2003

Eligibility

Ages Eligible for Study:  18 Years   -   76 Years,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • History of diabetes for at least 5 years, with a least 2 risk factors (i.e. hypertension, elevated cholesterol levels, history of or current smoker, obese, family history of heart disease) & atypical chest pain.

Exclusion Criteria:

  • Typical chest pain being treated with medication, unable to exercise, previous confirmed heart disease

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00162344

BMS Call Center      1 866 892 1BMS  Ext. 200 

California
      Local Institution, Rancho Santa Fe,  California,  United States; Recruiting

      Local Institution, Mission Viejo,  California,  United States; Recruiting

Illinois
      Local Institution, Winfield,  Illinois,  United States; Recruiting

Indiana
      Local Institution, Indianapolis,  Indiana,  United States; Recruiting

Minnesota
      Local Institution, St. Paul,  Minnesota,  United States; Recruiting

New York
      Local Institution, Albany,  New York,  United States; Recruiting

Canada, Quebec
      Local Institution, Montreal,  Quebec,  Canada; Recruiting

Study chairs or principal investigators

Martin Rosenberg, MD,  Principal Investigator,  Bristol Myers Squibb Medical Imaging   

More Information

Study ID Numbers:  CARDIOLITE-404
Last Updated:  September 12, 2005
Record first received:  September 9, 2005
ClinicalTrials.gov Identifier:  NCT00162344
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-13


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September 5, 2008



Page Updated: October 3, 2005
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