At a glance
ClinicalIndex Comparison RecordN/ACompleted· 294 enrolled
Drug / intervention
The Q-Fix™ All-Suture Anchordevice
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.
Safety and Performance of Q-Fix™ All-Suture Anchor System
In Brief
An observational study evaluating The Q-Fix™ All-Suture Anchor for Bankart Lesion and 15 related conditions. Completed, enrolled 294 participants across 5 sites.
Detailed Summary
Post-market clinical follow-up needed to address existing clinical data and gaps on the existing Q-Fix™ device and meet existing MDD/MEDDEV requirements
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsBankart Lesion, Acetabular Labrum Tear, SLAP Lesion, Acromioclavicular Sprain, Capsular Shift/Capsulolabral Reconstruction, Deltoid Repair, Rotator Cuff Repair, Bicep Tendinitis, Extra-capsular Repair, Medial Collateral Ligament, Lateal Collateral Ligament, Posterior Oblique Ligament, IBT, Vastus Medialis, Obliquus Advancement, Joint Capsule Closure
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
First PostedJul 2018
Enrollment StartAug 2018
Primary CompletionDec 2019
TodayJul 2026
First PostedJul 20, 2018
Enrollment StartAug 31, 2018
Primary CompletionDec 11, 2019
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 8.0 years ago
Interventions
The Q-Fix™ All-Suture Anchordevice
Observational, post-market, clinical follow-up study