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Sponsored by: |
Sheba Medical Center |
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Information provided by: | Sheba Medical Center |
ClinicalTrials.gov Identifier: | NCT00260377 |
Aspirin was proved to be the drug preventing vein grafts from closure and improving clinical outcome after coronary artery bypass surgery. It appears to be effective when being prescribed as early as first 48 hr. after the operation without increasing the incidence of bleeding complications. the exact effective dose is not known.
Condition | Intervention |
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Ischemic Heart Disease |
Procedure: Coronary artery bypass surgery |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Dose Comparison, Parallel Assignment |
Study Start Date: | January 2005 |
Estimated Study Completion Date: | December 2006 |
Estimated Primary Completion Date: | June 2006 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 30 Years to 90 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | SHEBA-03-3107-JL-CTIL |
Study First Received: | November 29, 2005 |
Last Updated: | September 8, 2008 |
ClinicalTrials.gov Identifier: | NCT00260377 |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
Aspirin treatment Aspirin resistance Coronary bypass surgery |
Heart Diseases Aspirin Myocardial Ischemia Vascular Diseases Ischemia |
Cardiovascular Diseases |