Status:
UNKNOWN
Analysis of Human Coronary Aspirate
Lead Sponsor:
Universität Duisburg-Essen
Conditions:
Coronary Arteriosclerosis
Coronary Heart Disease
Eligibility:
All Genders
Brief Summary
During elective percutaneous coronary intervention (PCI), both proximal and distal protection devices are used. The distal occlusion protection device temporarily occludes the vessel distal to the les...
Detailed Description
Patients * Symptomatic patients with a significant stenosis (diameter stenosis \>75% or significant FFR) in a native coronary vessel or a saphenous vein aortocoronary bypass graft. * All patients are...
Eligibility Criteria
Inclusion
- Symptomatic patients with a significant stenosis (diameter stenosis \>75% or significant FFR) in a native coronary vessel or a saphenous vein aortocoronary bypass graft
Exclusion
- Patients whereby a distal balloon occlusion devices is not applicable
Key Trial Info
Start Date :
April 1 2004
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
November 1 2015
Estimated Enrollment :
500 Patients enrolled
Trial Details
Trial ID
NCT01430884
Start Date
April 1 2004
End Date
November 1 2015
Last Update
December 3 2014
Active Locations (1)
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1
Center of Internal Medicine, University of Essen Medical School
Essen, Germany, 45122