RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System
Completed
Conditions studied: Peripheral Vascular Disease, Cardiovascular Disease
In brief
To evaluate early ambulation in patients who receive the StarClose™ VCS post-percutaneous diagnostic procedure.
Key facts
- Study ID
- NCT00736086
- Run by
- Abbott Medical Devices
- People needed
- 165
- Starts
- 2006-03-01
- Expected to finish
- 2006-12-01
- Last updated by the study team
- 2008-08-15
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Scripps Memorial Hospital — La Jolla, California, United States
- Fuqua Heart Center/ Piedmont Hospital — Atlanta, Georgia, United States
- Heart Care Midwest (OSF/St Francis) — Peoria, Illinois, United States
- The Care Group LLC (St. Vincent's Hospital) — Indianapolis, Indiana, United States
- Bay Regional Medical Center — Bay City, Michigan, United States
- Minneapolis Heart Institute Foundation/Abbott Northwestern Hospital — Minneapolis, Minnesota, United States
- St. Luke's Hospital — Kansas City, Missouri, United States
- New York Methodist Hospital — Brooklyn, New York, United States
- Buffalo Heart group — Buffalo, New York, United States
- North Ohio Research LTD Elyria Regional Medical — Elyria, Ohio, United States
- Drexel University College of Medicine Hahnemann — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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