Computed Tomography Coronary Angiography (CTCA) and Coronary Flow in Stenosis Analysis

NCT ID: NCT00921440

Last Updated: 2009-06-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-08-31

Study Completion Date

2008-07-31

Brief Summary

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The investigators' rationale was to evaluate whether a 64-slice CT scanner allows accurate measurement of computed tomographic changes in coronary artery flow profiles and whether CT flow measurements are suitable for classifying the significance and hemodynamic relevance of a stenosis and thereby supplement as a functional parameter for morphological stenosis analysis.

Detailed Description

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A total of 50 patients prospectively underwent computed tomography coronary angiography (CTCA) in a multidetector CT scanner (Brilliance 64, Philips) ± 1 day before or after invasive coronary angiography (ICA). Immediately thereafter, 2 radiologists reviewed the imaging data to detect any vessel segments with morphology poorly evaluable by CTCA. A locally constant cyclical measurement was acquired in these coronary arteries in breath-hold technique during the passage of a 50ml bolus of contrast media. For analysis, time-density curves of the bolus passage were registered in the coronary artery and the aorta (internal reference), the up-slopes were determined and correlated with each other. The results were compared with the ICA findings.

Conditions

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Coronary Artery Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Clinically known or presumed CAD
* Age \> 50 years
* Hospitalization for invasive coronary angiography
* Sinus rhythm
* Written informed consent by the patient to participate in the study after comprehensive presentation of the facts

Exclusion Criteria

* Age \<= 50 years
* Contraindications to contrast media administration (medical history of iodine allergy, nephropathy, latent or manifest hyperthyroidism)
* Arrhythmias
* Dyspnea at rest, acute unstable angina pectoris, acute myocardial infarction
* Pregnancy
* Implanted pacemaker
* Unwillingness of patient to consent to the study
Minimum Eligible Age

51 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dept. of Radiology

UNKNOWN

Sponsor Role collaborator

University of Cologne

OTHER

Sponsor Role lead

Responsible Party

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University Hospital of Cologne, Dept. Radiology

Principal Investigators

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Barbara Krug, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

Dept. of Radiology, University Hospital of Cologne

Other Identifiers

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22462/2 - 2005-070

Identifier Type: -

Identifier Source: org_study_id

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