At a glance
ClinicalIndex Comparison RecordN/ACompleted· 356 enrolled
Drug / intervention
GORE® PROPATEN® Vascular Graft +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Retrospective Post-Market Clinical Follow-Up Study of GORE-TEX® Vascular Grafts and GORE® PROPATEN® Vascular Graft in Peripheral Artery Disease, Aortic Aneurysms, and Dialysis Access
In Brief
An observational study evaluating GORE® PROPATEN® Vascular Graft and GORE-TEX® Vascular Grafts for PAD - Peripheral Arterial Disease and 2 related conditions. Completed, enrolled 356 participants across 8 sites in 3 countries.
Detailed Summary
This multicenter, single-arm retrospective registry (chart review) is being conducted to confirm the clinical performance and safety of GORE-TEX® Vascular Grafts and GORE® PROPATEN® Vascular Graft throughout the device functional lifetime for each indication area.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPAD - Peripheral Arterial Disease, AAA - Abdominal Aortic Aneurysm, End-Stage Renal Disease
CountriesFrance, Italy, Spain
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
First PostedNov 2021
Enrollment StartJan 2022
Primary CompletionJul 2024
TodayJul 2026
First PostedNov 17, 2021
Enrollment StartJan 24, 2022
Primary CompletionJul 22, 2024
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 4.6 years ago
Interventions
GORE® PROPATEN® Vascular Graftdevice
Patients that have had treatment with GORE® PROPATEN® Vascular Graft
GORE-TEX® Vascular Graftsdevice
Patients that have had treatment with GORE-TEX® Vascular Grafts