The Vascutek Rapidax™ II Post Market Surveillance Registry
NCT01977508 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 24
Last updated 2016-05-20
Summary
Multicentre, prospective, observational post-market registry. To monitor and collect data on the post-market clinical safety and performance of the Vascutek Rapidax II Vascular Access Graft.
Conditions
Interventions
- DEVICE
-
ePTFE vascular access grafts
Sponsors & Collaborators
-
Vascutek Ltd.
lead INDUSTRY
Principal Investigators
-
Bernd Lobenstein · Saale-Unstrut Klinikum Naumburg
Eligibility
- Min Age
- 18 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-08-31
- Primary Completion
- 2016-05-31
- Completion
- 2016-05-31
Countries
- Germany
Study Locations
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