MDR SureLock All-Suture Anchor
Last updated on July 2021Recruitment
- Recruitment Status
- Enrolling by invitation
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Labral Tear, Glenoid
- Shoulder Disease
- Shoulder Injuries
- Shoulder Pain
- Shoulder Pain Chronic
- Shoulder Syndrome
- Design
- Observational Model: CohortTime Perspective: Other
Participation Requirements
- Age
- Between 14 years and 45 years
- Gender
- Both males and females
Description
Patient-reported outcomes data have been collected among patients undergoing shoulder labrum repair with SureLock all-suture anchors from January 2014 to June 30, 2020. These patients have completed clinical and quality-of-life outcome instruments pre-operatively, and have been stored securely in th...
Patient-reported outcomes data have been collected among patients undergoing shoulder labrum repair with SureLock all-suture anchors from January 2014 to June 30, 2020. These patients have completed clinical and quality-of-life outcome instruments pre-operatively, and have been stored securely in the OBERD database. Pre-op scores will be compared to post-op scores and analyzed using a one-way ANOVA test with a post-hoc Scheffe procedure. Patient identifying information will be removed and de-identified codes will be used. Any new prospective data gathered prospectively for the purposes of this study will be entered and stored securely as above. Data collection forms will consist of the following Patient-Reported Outcome Surveys: WOSI Index, ASES Shoulder Score, and the SF-12.
Tracking Information
- NCT #
- NCT04093700
- Collaborators
- Not Provided
- Investigators
- Study Director: Kacy Arnold, MBA, RN Zimmer Biomet
Get Well Soon