At a glance
ClinicalIndex Comparison RecordN/ACompleted· 213 enrolled
Drug / intervention
Tack Endovascular Systemdevice
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.
Tack Optimized Balloon Angioplasty Study for Superficial Femoral and Proximal Popliteal Arteries Using the Tack Endovascular System™
In Brief
A clinical study evaluating Tack Endovascular System for Peripheral Artery Disease. Completed, enrolled 213 participants across 39 sites in 3 countries.
Detailed Summary
This is a prospective, multi-center, single-arm, non-blinded study designed to investigate the safety and efficacy of the Tack Endovascular System in subjects with post-balloon angioplasty (post-PTA) dissection(s) type(s) A through F in the superficial femoral and proximal popliteal arteries ranging in diameter from 2.5mm to 6.0mm.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPeripheral Artery Disease
CountriesAustria, Netherlands, United States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedAug 2015
Enrollment StartSep 2015
Primary CompletionMay 2018
Study CompletionMar 2020
TodayJul 2026
First PostedAug 13, 2015
Enrollment StartSep 1, 2015
Primary CompletionMay 1, 2018
Study CompletionMar 1, 2020
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 10.9 years ago
Interventions
Tack Endovascular Systemdevice
Repair of post-PTA dissections using the Intact Vascular Tack Endovascular System.