Rotation Medical Bioinductive Implant Database Registry (REBUILD)

Smith & Nephew

Status: Completed

Conditions: Rotator Cuff Tear

Treatments: Device: Bioinductive implant

Study type: Observational

Funder types: Industry

Identifiers

NCT02784600

3679-01

Details and patient eligibility

About

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.

Enrollment: 483 patients

Sex: All

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. At least 21 years of age.
2. Able and willing to provide voluntary consent to Registry participation.
3. Able to read, speak, and understand the English language.

Exclusion criteria

1. Hypersensitive to bovine-derived materials.

Trial design

483 participants in 1 patient group

Partial or full-thickness rotator cuff tear

Description:

Rotation Medical bioinductive implant

Treatment:

Device: Bioinductive implant