At a glance
ClinicalIndex Comparison RecordN/ACompleted· 233 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 the Below The Knee Arteries Using the Tack Endovascular System®
In Brief
A clinical study evaluating Tack Endovascular System for Peripheral Arterial Disease. Completed, enrolled 233 participants across 49 sites in 6 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 the Mid/Distal Popliteal, Tibial, and Peroneal Arteries ranging in diameter from 1.5mm to 4.5mm for the treatment of post percutaneous transluminal balloon angioplasty (PTA) dissection(s) requiring repair.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPeripheral Arterial Disease
CountriesAustria, Czechia, Germany, Hungary, New Zealand, United States
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedOct 2016
Enrollment StartFeb 2017
Primary CompletionJul 2019
Study CompletionJan 2022
TodayJul 2026
First PostedOct 24, 2016
Enrollment StartFeb 8, 2017
Primary CompletionJul 11, 2019
Study CompletionJan 10, 2022
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 9.7 years ago
Interventions
Tack Endovascular Systemdevice
Repair of post-PTA dissections using the Intact Vascular Tack Endovascular System.