Status:
TERMINATED
Outpatient Percutaneous Coronary Intervention
Lead Sponsor:
University of Pennsylvania
Collaborating Sponsors:
Abbott Medical Devices
The Medicines Company
Conditions:
Coronary Artery Disease
Eligibility:
All Genders
18-75 years
Brief Summary
To determine the safety and feasibility of same day discharge after elective coronary percutaneous intervention in a selected stable patient population. The hypothesis to be tested is that in an appro...
Detailed Description
A select stable population of patients undergoing percutaneous coronary intervention are randomized to standard of care in-hospital stay for one night or early discharge to a nearby hotel. During PCI,...
Eligibility Criteria
Inclusion
- Patients with stable coronary artery disease scheduled for elective percutaneous coronary intervention
Exclusion
- Patients with acute coronary syndrome, patients with an MI within 30 days, an ejection fraction \<30%, those with history of IV Dye allergy, creatinine level\>2.2, those with increased risk of infection, those with history of bleeding diathesis or anemia (hemoglobin\<11.0 g/dl, platelets \<100,000 tho/ul)
Key Trial Info
Start Date :
August 1 2004
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
August 1 2006
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00419055
Start Date
August 1 2004
End Date
August 1 2006
Last Update
April 2 2012
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