Outcome of Rotator Cuff Repair using Acellular Dermal Matrix Augmentatio

Not Applicable

• Conditions: Diseases of the musculo-skeletal system and connective tissue

• Registration Number: KCT0005946
• Lead Sponsor: Samsung Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 March 2021

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 61

Inclusion Criteria

(1) Large or massive rotator cuff tear requiring rotator cuff repair
(2) The patients with defect at tendon insertion during arthroscopic rotator cuff repair

Exclusion Criteria

(1) Previous surgery history at affected shoulder
(2) Previous fracture history at affected shoulder
(3) Previous infection history at affected shoulder
(4) Prmiary or secondary osteoarthritis
(5) Indication for reverse shoulder arthroplasty because of advanced cuff tear arthropathy of shoulder joint
(6) Massive rotator cuff tear requiring superior capsule reconstruction
(7) Patients with neurological symptoms, inability to follow postoperative instructions, or non-cooperative
(8) Patients judged to be difficult to participate in the study due to cognitive impairment

Study & Design

• Study Type: Observational Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rotator cuff retear rate using MRI

Secondary Outcome Measures

Name	Time	Method
American Shoulder and Elbow Surgeons Shoulder (ASES) score, range of motion of shoulder