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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00352937
Other study ID # 1124528
Secondary ID
Status Completed
Phase Phase 3
First received July 14, 2006
Last updated May 14, 2014
Start date March 2006
Est. completion date December 2009

Study information

Verified date May 2014
Source Providence VA Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

To compare the efficacy of 16-row multi-detector CT (MDCT) with standard myocardial perfusion imaging in detecting coronary artery disease (CAD) in patients without a previously established diagnosis of CAD.


Description:

Nuclear stress testing is currently the established non-invasive modality in detecting flow-obstructing coronary artery disease (CAD).

Recently, multi-detector CT (MDCT) has emerged as a new modality that offers a non-invasive means to directly visualize coronary anatomy and any CAD. Studies have shown that MDCT has excellent sensitivity and a high negative predictive value in detecting significant CAD.

The purpose of this study is to compare MDCT with nuclear stress testing for detecting CAD in previously undiagnosed patients.


Recruitment information / eligibility

Status Completed
Enrollment 98
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Referred for a clinical indicated stress SPECT MPI

- Adequate IV access in both arms

Exclusion Criteria:

- History of coronary angioplasty or stent placement

- History of coronary bypass surgery

- Angiographic history of flow-limiting CAD

- Documented history of elevated cardiac markers

- Documented history of injury or infarct on ECG

- Absence of sinus rhythm

- Current history of renal insufficiency

- Known allergy to contrast dye

- Pregnant

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
United States Providence Veterans Affairs Medical Center Providence Rhode Island

Sponsors (1)

Lead Sponsor Collaborator
Providence VA Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Calcium score 1 year No
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