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

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBrooke Army Medical Center

About this trial

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.

Eligibility criteria

Qualifiers

DEERS-eligible

Adults, between the ages of 18-65 (inclusive)

Presenting with a rotator cuff tear that is reparable surgically (a reparable tear is defined as tear of the RC where it is possible to bring the retracted tendon edge back to the greater tuberosity of the humerus under minimal tension)

Ability to undergo surgery to repair rotator cuff tear

Disqualifiers

Previous shoulder surgery (excluding acromioplasty or diagnostic arthroscopy)

Inability to receive an MRI

Current (within the past 6 months) tobacco user

Unwilling to remain tobacco free for the duration of the study

Trial design

Treatments tested in this trial

  • Rotator cuff repairs with BioEnthesis augmentation
  • Rotator cuff repairs without BioEnthesis augmentation

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Brooke Army Medical Center

Lead sponsor

Sparta Biopharma

Collaborator

Musculoskeletal Injury Rehabilitation Research for Operational Readiness

Collaborator