At a glance
ClinicalIndex Comparison RecordN/ACompleted· 100 enrolled
Drug / intervention
CTO crossing in femoropopliteal arteries CONNECT IIdevice
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.
A Non-randomized Study of the Avinger Ocelot System Used to Cross Chronic Total Occlusions in the Superficial Femoral and Popliteal Arteries
In Brief
A clinical study evaluating CTO crossing in femoropopliteal arteries CONNECT II for Total Atherosclerotic Occlusion of Femoral Artery. Completed, enrolled 100 participants across 17 sites in 3 countries.
Detailed Summary
Evaluation of the safety and effectiveness of the Ocelot System to provide OCT-assisted orientation while simultaneously crossing totally occluded femoropopliteal arteries.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany, Italy, United States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartFeb 2012
First PostedFeb 2012
Primary CompletionJun 2012
TodayJul 2026
First PostedFeb 23, 2012
Enrollment StartFeb 1, 2012
Primary CompletionJun 1, 2012
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 14.4 years ago
Interventions
CTO crossing in femoropopliteal arteries CONNECT IIdevice
CTO crossing in femoropopliteal arteries using the Ocelot System