- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01779986
Comparison of the Evaluation of CAD by CT AngioScan and Coronary Angiogram (CTAS-MCAS)
January 29, 2013 updated by: Université de Sherbrooke
Comparison of the Evaluation of CAD by CT AngioScan and Coronary Angiogram in Patient as Part of Preoperative Evaluation in Ascending Aorta Replacement Surgery Patients.
The use of CT Coronary Angioscan (CT-AS) is gaining popularity, but its exact value as evaluation of CAD requires confirmation.
We intend to compare the results of CT-AS and convention coronary angiogram results in patients who are scheduled for an ascending aorta aneurysm reparation surgery.
These examens are standard of care before this surgery, so there is no additional danger or disadvantage for the patient.
We hope to confirm that CT-AS is a reliable screening test for CAD in patient undergoing heart surgery for other reason than CAD.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Quebec
-
Sherbrooke, Quebec, Canada, J1H 5N4
- Recruiting
- CHUS Fleurimont
-
Contact:
- Paul Farand, M.Sc
- Phone Number: 819-346-1110
- Email: paul.farand@sherbrooke.ca
-
Principal Investigator:
- Gérald Gahide, MD
-
Sub-Investigator:
- Paul Farand, MD, MSc
-
Sub-Investigator:
- Tamas Z Fulop, MD
-
Sub-Investigator:
- Francis Rivest, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 89 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients with ascending aorta aneurysm undergoing preoperative evaluation of CAD by CT-Angioscan and Coronary angiogramm before surgical reparation.
Description
Inclusion Criteria:
- Ascending aorta aneurysm waiting for surgical correction
- Willing to participate
- Needing a Coronary angiogram and a CT-AS for medical reasons
Exclusion Criteria:
- Refuse to participate
- Allergy to contrast material
- Incomplete results or having one of the test done in another hospital
- Arrythmia
- More than 6 months between the two exams
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Presence of CAD
Time Frame: less than 6 monthes between two tests
|
The CAD seen on CT-AS as compared to the results of the gold-standard test of coronary angiogram.
|
less than 6 monthes between two tests
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gerald Gahide, MD PHD, Université de Sherbrooke
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2013
Primary Completion (Anticipated)
February 1, 2015
Study Completion (Anticipated)
February 1, 2015
Study Registration Dates
First Submitted
January 28, 2013
First Submitted That Met QC Criteria
January 29, 2013
First Posted (Estimate)
January 30, 2013
Study Record Updates
Last Update Posted (Estimate)
January 30, 2013
Last Update Submitted That Met QC Criteria
January 29, 2013
Last Verified
January 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CTAS-MCAS UdeS 12-073
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.