CompletedPhase 3NCT00737672
GORE VIABAHN Endoprosthesis Versus Percutaneous Transluminal Angioplasty (PTA) to Revise AV Grafts in Hemodialysis
Studying Complication in hemodialysis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- W.L.Gore & Associates
- Principal Investigator
- Tom Vesely, MD, M.DVascular Access Center; Frontenac, MO
- Intervention
- GORE VIABAHN Endoprosthesis with PROPATEN Bioactive Surface(device)
- Enrollment
- 293 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2008 – 2013
Study locations (29)
- Birmingham, Alabama, United States
- Fresno, California, United States
- Inglewood, California, United States
- Oceanside, California, United States
- Riverside, California, United States
- San Diego, California, United States
- San Francisco, California, United States
- New Haven, Connecticut, United States
- Jacksonville, Florida, United States
- Albany, Georgia, United States
- Chicago, Illinois, United States
- Des Moines, Iowa, United States
- Louisville, Kentucky, United States
- Baltimore, Maryland, United States
- New Brighton, Minnesota, United States
- +14 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT00737672 on ClinicalTrials.govOther trials for Complication in hemodialysis
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