Groin Complications Post Percutaneous Coronary Intervention Using Either Manual Compression or PERCLOSE Device
Completed
Conditions studied: Vascular Closure
In brief
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 device (VCD) or manual compression.
Key facts
- Study ID
- NCT00842179
- Run by
- Clinyx, LLC
- People needed
- 2517
- Starts
- 2008-06-01
- Expected to finish
- 2008-10-01
- Last updated by the study team
- 2009-02-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Patients less than 18 years old
Where it is running
- Baptist Hospital of Miami — Miami, Florida, United States
Full record on ClinicalTrials.gov
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