Demineralized Bone Matrix Rotator Cuff Study

Status Active, not recruiting

Clinical Trial Summary

Patients undergoing rotator cuff repair surgery will experience improved tendon healing with the use of demineralized bone matrix augmentation.

Clinical Trial Description

This is a prospective randomized study comparing the outcomes of patient undergoing rotator cuff repair with either an interpositional procedure administering demineralized bone matrix (DBM), or a control group without demineralized bone matrix. Patient outcomes will be collected and compared between the two cohorts up to a five (5) year post-operative period and will include a range of subjective and functional outcomes, along with radiographic imaging. ;

Study Design

Related Conditions & MeSH terms

Rotator Cuff Injuries

Clinical Trial Details

NCT number	NCT04686396
Study type	Interventional
Source	Arthrex, Inc.
Contact
Status	Active, not recruiting
Phase	N/A
Start date	September 1, 2019
Completion date	September 2024

View Details

See also
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