Trials / Completed
CompletedNCT02784600
Rotation Medical Bioinductive Implant Database Registry
Rotation MEdical BioindUctive ImpLant Database (REBUILD) Registry
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 483 (actual)
- Sponsor
- Smith & Nephew, Inc. · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this clinical registry is to prospectively collect and compare preoperative and postoperative patient-reported data using validated shoulder-specific and health-related quality of life (QoL) instruments during real-world use of the Rotation Medical bioinductive implant to treat rotator cuff tears.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Bioinductive implant |
Timeline
- Start date
- 2016-04-25
- Primary completion
- 2020-01-16
- Completion
- 2020-01-16
- First posted
- 2016-05-27
- Last updated
- 2021-10-18
Locations
19 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02784600. Inclusion in this directory is not an endorsement.