This trial is active, not recruiting.

Condition full thickness rotator cuff tear
Treatments augment rotator cuff, standard suture repair
Phase phase 1
Sponsor BioMimetic Therapeutics
Start date November 2010
End date June 2011
Trial size 30 participants
Trial identifier NCT01256242, BMTI-2010-03


Study Purpose: To evaluate the safety and performance of Augment Rotator Cuff as a primary surgical treatment for full thickness rotator cuff tears. The hypothesis is that Augment Rotator Cuff will be easy to deliver as an inter-positional graft placed between the rotator cuff tendon and the humeral head providing further enhanced tendon to bone healing without adding any additional safety risk to the patient.

Study Rationale: To evaluate the safety and performance Augment™ Rotator Cuff in surgical intervention of a torn rotator cuff and to obtain preliminary data to support the rationale for a subsequent pivotal clinical trial.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety study
Intervention model parallel assignment
Masking single blind (outcomes assessor)
Primary purpose treatment
Standard Suture Repair + Augment Rotator Cuff
augment rotator cuff
rhPDGF-BB and bovine collagen matrix
(Active Comparator)
Standard Suture Repair
standard suture repair
standard suture repair

Primary Outcomes

time frame: 24 weeks
time frame: 24 weeks

Secondary Outcomes

Clinical Outcome Measurements
time frame: 24 weeks
time frame: 24 weeks

Eligibility Criteria

Male or female participants at least 21 years old.

Inclusion Criteria: - The subject has a repairable rotator cuff tear with an estimated full thickness size of ≥ 2 cm to < 5 cm confirmed with diagnostic MRI in AP or ML dimension - The subject is independent, ambulatory, and can comply with all post-operative evaluations and visits - The subject is at least twenty one (21) years of age and considered to be skeletally mature. Exclusion Criteria: - The subject has undergone previous rotator cuff repair surgery to the affected shoulder - The subject has a partial thickness rotator cuff tear - The subject requires a concomitant subscapularis repair - The subject requires a concomitant labral repair - The subject has an irreparable rotator cuff tear - The subject has an allergy to yeast-derived products or a known bovine collagen allergy - The subject has implanted metallic devices (cardiac pacemakers, insulin pumps, and nerve stimulators), medically implanted clips or other electronically, magnetically or mechanically activated implants that would contraindicate undergoing an MRI scan of the shoulder - The subject has tested positive or has been treated for a malignancy in the past or is suspected of having a malignancy or is currently undergoing radiation or chemotherapy treatment for a malignancy anywhere in the body, whether adjacent to or distant from the proposed Augment Rotator Cuff implantation site - The subject's condition represents a worker's compensation case - The subject is currently involved in a health-related litigation procedure - The subject is pregnant or able to become pregnant but not practicing a medically-accepted form of birth control, and/or intending to become pregnant during this study period

Additional Information

Official title A Single Blinded, Multi-center, Randomized, Controlled, Pilot Study to Evaluate the Safety and Performance of Augment™ Rotator Cuff for Primary Surgical Treatment of Full Thickness Rotator Cuff Tears
Principal investigator Robert Litchfield, MD, FRCSC
Trial information was received from ClinicalTrials.gov and was last updated in May 2011.
Information provided to ClinicalTrials.gov by BioMimetic Therapeutics.