- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00709709
Medical Evaluation of Scanner in Coronary Syndrome (EVASCAN)
Medical and Economic Medical Evaluation of Scan Multislice of Coronary Artery in Exploration of Stable Coronary Syndrome. Comparison With Quantitative Coronarography
Many recent publications have reported encouraging results on diagnostic cardiac multislice CT performance in 1) coronary artery disease, 2) coronary arterial bypass graft potency and 3) intrastent restenosis.
These single center studies were made on a limited number of patients (range, 50-130) and focused mainly on one of the indications mentioned above.
Moreover, results were often given after exclusion of low quality examinations. At last, no study has compared the diagnostic performance of the different CT systems '16, 40 and 64) in these populations.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
These single center studies were made on a limited number of patients (range, 50-130) and focused mainly on one of the indications mentioned above.
Moreover, results were often given after exclusion of low quality examinations. At last, no study has compared the diagnostic performance of the different CT systems '16, 40 and 64) in these populations.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Creteil, France, 94
- CHU Henri Mondor
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients' ≥18 years, of both sexes
- Coronary angiography in patients with suspected of known CAD, instable clinical conditions.
- Clinical status allowing performance of coronary angiography 48 à 72h after CT examination
- Informed consent signed by patient
Exclusion Criteria:
- Patients in whom clinical status does not allow delayed coronary angiography
- Irregular heart rate, in particular atrial fibrillation
- Renal insufficiency (serum creatinine >150 µmol/l
- Radiology examination with use of iodin agent with 48h before) CT coronary
- K now intolerance to iodin agents
- Patients unable to hold breathing < 20 seconds
- Pregnancy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: 1
Scan
|
multislice coronary scan
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Specificity and sensibility of scanner
Time Frame: visit 1
|
visit 1
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Quality of coronary scanner imaging
Time Frame: visit 1
|
visit 1
|
Collaborators and Investigators
Investigators
- Principal Investigator: Pascal Gueret, PUPH, Assistance Publique - Hôpitaux de Paris
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P060105
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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