Prospective Study to Determine the Safety and Effectiveness of a Connective Tissue Allograft Active Matrix (AM) Vs. Standard of Care in Arthroscopic Rotator Cuff Repair

Recruiting

AM vs. Standard of CareProspective Study to Determine the Safety and Effectiveness of a Connective Tissue Allograft Active Matrix (AM) Vs. Standard of Care in Arthroscopic Rotator Cuff Repair

Sponsor:

The University of Texas Health Science Center, Houston

Code:

NCT05894265

Conditions

Rotator Cuff Tears

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

ActiveMatrix® Dosage A

ActiveMatrix® Dosage B

Saline injection

Study Details

Eligibility Criteria

Study Design

Interventions and Outcome Measures

Central Contacts and Locations

More Information

Trial information was received from ClinicalTrials.gov and was last updated on 2025-05-09. This information was provided to ClinicalTrials.gov by The University of Texas Health Science Center, Houston on 2025-02-21.