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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01896674
Other study ID # Kuma1478
Secondary ID
Status Completed
Phase N/A
First received July 8, 2013
Last updated July 10, 2013
Start date May 2012

Study information

Verified date July 2013
Source Kumamoto University
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study was to compare FBP-, hybrid IR-, and IMR techniques to assess their role in the identification of coronary artery disease and abnormalities in cardiac structures.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date
Est. primary completion date January 2013
Accepts healthy volunteers No
Gender Both
Age group 45 Years to 85 Years
Eligibility Inclusion Criteria:

- A BMI of 27 kg/m2 or less and a coronary calcium score of less than 1,000 Agatston units.

Exclusion Criteria:

- BMI exceeded 27 kg/m2

- renal dysfunction (serum creatinine level > 1.5 mg/dl)

- atrial fibrillation

- prior coronary artery bypass grafting

- heart failure (New York Heart Association class III-IV)

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Kumamoto University

Outcome

Type Measure Description Time frame Safety issue
Primary Contrast to noise ratio of coronary arteries 6 months No
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