MedTrace Logo

MDR SureLock All-Suture Anchor

NCT04093700 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2023-08-14

No results posted yet for this study

Summary

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.

Conditions

  • Shoulder Pain
  • Shoulder Injuries
  • Shoulder Disease
  • Shoulder Pain Chronic
  • Shoulder Syndrome
  • Labral Tear, Glenoid

Interventions

DEVICE

SureLock All-Suture Anchor

Subjects that have been implanted with the SureLock All-Suture Anchor to repair the glenoid labrum

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Eligibility

Min Age
14 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-05
Primary Completion
2022-11-08
Completion
2022-11-08
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04093700 on ClinicalTrials.gov