Status:
COMPLETED
Peri-Operative Morbidity and Quality of Life After Coronary Artery Bypass Graft (CABG)
Lead Sponsor:
Weill Medical College of Cornell University
Collaborating Sponsors:
National Heart, Lung, and Blood Institute (NHLBI)
Conditions:
Coronary Artery Bypass Graft Surgery
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
It is the long term objective of this study to preserve or improve the quality of life and to prevent deterioration in physical and mental function following myocardial revascularization among bypass ...
Detailed Description
The objective of this study is to compare the efficacy of two strategies of intra-operative hemodynamic management in preventing peri-operative cardiac, cognitive and neurologic morbidity and mortalit...
Eligibility Criteria
Inclusion
- Patients had to be undergoing elective CABG, without concomitant valve or other cardiac surgery.
- Patients also had to be able to perform the neuropsychologic tests, and to provide informed consent.
Exclusion
- Patients who refused to participate in the study.
- Patients who live too far away from NYC to be able to come back for follow up at six months post-operatively.
- Patients who had either valvular replacement and aortic amd mitral an aneurysm repair, or other cardiothoracic surgery.
- Patients who were unable to complete the neuropsychologic test.
- Patient who were part of another CABG study.
Key Trial Info
Start Date :
September 1 1991
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 1994
Estimated Enrollment :
248 Patients enrolled
Trial Details
Trial ID
NCT00248885
Start Date
September 1 1991
End Date
September 1 1994
Last Update
April 11 2008
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
New York Presbyterian Hospital-Weill Cornell Medical College
New York, New York, United States, 10065