MDR SureLock All-Suture Anchor
TerminatedNCT04093700
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
To report the outcomes of a series of patients with recurrent anterior and/or posterior shoulder instability who underwent surgical repair of the affected labrum using the SureLock all-suture anchor.
Study details
- Official title
- Clinical Outcomes of Surgical Repair of the Glenoid Labrum Using an All-Suture Anchor
- Conditions
- Shoulder Pain
- Shoulder Injuries
- Shoulder Disease
- Shoulder Pain Chronic
- Shoulder Syndrome
- Labral Tear, Glenoid
- Interventions
- Device: SureLock All-Suture Anchor
- Sponsor
- Zimmer Biomet
- Start date
- 2019-11-05
- Primary completion
- 2022-11-08
- Sex
- All
- Age range
- from 14 Years to 45 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 14 to 45 years of age * Surgery performed between 1/1/14-12/31/2021 * Recurrent shoulder instability resulting from an isolated anterior and/or posterior glenoid labral tear * Completed pre-operative data (WOSI, ASES, SF-12) Exclusion Criteria: * Diagnosis of concomitant SLAP tear * Diagnosis of concomitant full-thickness rotator cuff tear * Greater than 10% loss of glenoid bone * Greater than 25% humeral head defect * Prior surgical intervention for the treatment of shoulder instability (in either the affected shoulder or the contralateral shoulder) * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Pregnant women * Prisoners
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04093700