Status:
TERMINATED
Evaluation of a Local Preconditioning Effect in Patients Undergoing Cardiac Surgery
Lead Sponsor:
Medical University of Vienna
Conditions:
Heart Disease
Coronary Artery Bypass Graft Triple Vessel
Eligibility:
All Genders
18-85 years
Phase:
NA
Brief Summary
The aim of the study is to analyze the potential of pressure controlled intermittent coronary sinus occlusion (PICSO) to prevent/reverse the ischemic burden as well as reperfusion injury. To achieve i...
Detailed Description
* Patients undergoing elective coronary artery bypass graft (CABG) will be enrolled in this study. * A computerized randomization process is used to obtain similar distributions within each group. Str...
Eligibility Criteria
Inclusion
- Adult patients of either sex and between 18 and 85 years of age scheduled for surgery without severe confounding disease will be asked to participate in the study.
- Written informed consent will be obtained in eligible patients.
Exclusion
- Patients with unstable angina pectoris and/or myocardial infarction within the last 30 days, as well as persons with planned concomitant valvular interventions will be excluded. Patients with malignoma, severe hepatic, renal and pulmonary disease will also be excluded
Key Trial Info
Start Date :
March 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2014
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT01482780
Start Date
March 1 2012
End Date
March 1 2014
Last Update
April 7 2015
Active Locations (1)
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1
Medical University of Vienna
Vienna, Vienna, Austria, A-1090