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NOT YET RECRUITING
NCT06289686
PHASE4

MIRROR Project 44 - Rotator Cuff Repairs With or Without BioEnthesis™ Augmentation

Sponsor: Brooke Army Medical Center

View on ClinicalTrials.gov

Summary

Rotator cuff (RC) injuries are particularly prevalent, difficult to repair, and attachment between the bone and tendon is notoriously difficult to achieve. The most common method and current standard of care (SOC) for reattaching connective tissues (e.g., ligaments, tendons) to bone typically involves suture anchor-based techniques, but this is fraught with problems. More specifically, re-tearing of the connective tissue after this procedure occurs in 30-60% of cases, and can be even higher in patients who engage in smoking, have a diagnosis of diabetes, etc. To address these clinical challenges, Sparta Biopharma Inc. (Sparta) developed a unique technology, called BioEnthesis, to improve the connection between the tendon and bone. Pre-clinical in vivo studies demonstrated that the biphasic bovine cancellous matrix regenerated at the bone-soft tissue interface-thereby leading to high structural integrity and will likely lead to reduced re-tear rates over time. The investigators hypothesize that patients in this interventional cohort will experience enhanced mobility, reduced pain, and less re-tears after RC procedures versus a standard suture anchor-based repair.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-07

Completion Date

2025-12

Last Updated

2024-06-07

Healthy Volunteers

No

Interventions

PROCEDURE

Rotator cuff repairs with BioEnthesis augmentation

Rotator cuff repair using BioEnthesis allograft patch

PROCEDURE

Rotator cuff repairs without BioEnthesis augmentation

Rotator cuff repair using standard of care sutures and anchors

Locations (2)

Walter Reed National Military Medical Center

Bethesda, Maryland, United States

Brooke Army Medical Center

San Antonio, Texas, United States