At a glance
ClinicalIndex Comparison RecordN/ACompleted· 148 enrolled
Drug / intervention
Bioinductive implant +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.
Post-Market Evaluation of the Rotation Medical Rotator Cuff System
In Brief
A clinical study evaluating Bioinductive implant and Surgical repair for Partial Thickness Supraspinatus Tendon Tear and Full Thickness Supraspinatus Tendon Tear. Completed, enrolled 148 participants across 15 sites.
Detailed Summary
The purpose of this study is to evaluate bioinduction of new tissue and tendon healing after implantation of the Rotation Medical Bioinductive Implant used as either a standalone device or adjunct to surgical repair in the treatment of supraspinatus tendon tears.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJul 2014
Enrollment StartAug 2014
Primary CompletionNov 2020
TodayJul 2026
First PostedJul 25, 2014
Enrollment StartAug 20, 2014
Primary CompletionNov 24, 2020
TodayJul 2, 2026
Enrollment to primary: 6.3 yearsPosted 11.9 years ago
Interventions
Bioinductive implantdevice
Surgical repairdevice
Surgical repair with commercially-available sutures/suture anchors.