Status:
COMPLETED
Groin Complications Post Percutaneous Coronary Intervention Using Either Manual Compression or PERCLOSE Device
Lead Sponsor:
Clinyx, LLC
Collaborating Sponsors:
Abbott Medical Devices
Conditions:
Vascular Closure
Eligibility:
All Genders
18+ years
Brief Summary
The objective of this study is to compare groin complication rates in low and high risk patients post percutaneous coronary intervention (PCI) closed by either a 6 French Perclose vascular closure dev...
Detailed Description
It is commonly accepted that that there exists a learning curve in performing successful groin closure with Vascular Closure Devices (VCD). Manual compression continues to be 'standard of care' at mos...
Eligibility Criteria
Inclusion
- Patients who received vascular closure with the Perclose device post PCI at Baptist Miami Hospital
- Patients who received vascular closure by manual compression at Tampa General Hospital
Exclusion
- Patients less than 18 years old
Key Trial Info
Start Date :
June 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2008
Estimated Enrollment :
2517 Patients enrolled
Trial Details
Trial ID
NCT00842179
Start Date
June 1 2008
End Date
October 1 2008
Last Update
February 12 2009
Active Locations (1)
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1
Baptist Hospital of Miami
Miami, Florida, United States, 33176