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Clinical Trials/NCT00001633
NCT00001633
Completed
Phase 2

A Phase II Feasibility Study of the Safety and Efficacy of Coronary Magnetic Resonance Angiography (CMRA) Imaging

National Heart, Lung, and Blood Institute (NHLBI)1 site in 1 country20 target enrollmentSeptember 1997

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Coronary Disease
Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Enrollment
20
Locations
1
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

Magnetic resonance imaging (MRI) is a diagnostic tool that creates high quality images of the human body without the use of X-ray (radiation). MRI is especially useful when studying the arteries of the heart (CMRA, coronary magnetic resonance angiography).

In this study researchers from several laboratories and hospitals will work together to determine the safety and effectiveness of CMRA with MS-325. MS-325 is a contrast agent. It is given to patients undergoing CRMA in order to improve the appearance of the arteries of the heart.

Detailed Description

In this multicenter trial, the safety and efficacy of magnetic resonance imaging (MRI) for visualization of the coronary arteries (CMRA, coronary magnetic resonance angiography) with MS-325. MS-325 is a new blood pool radiological contrast agent which will be assessed as part of a phase II feasibility study. The Laboratory of Cardiac Energetics in collaboration with the Department of Cardiology at the George Washington Hospital Center will be one of the six participating sites for this study.

Registry
clinicaltrials.gov
Start Date
September 1997
End Date
December 2000
Last Updated
18 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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