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Outcome of Rotator Cuff Repair using Acellular Dermal Matrix Augmentation

Clinical and Radiological Outcome Study of Arthroscopic Hybrid Rotator Cuff Repair with Acellular Dermal Matrix Augmentation in Large to Massive Rotator Cuff Tear

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0005946
Enrollment
61
Registered
2021-03-03
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Rotator cuff retear rate using MRI—

Secondary

MeasureTime frame
American Shoulder and Elbow Surgeons Shoulder (ASES) score, range of motion of shoulder—

Countries

Korea, Republic of

Contacts

Public ContactSu Cheol Kim

Samsung Medical Center

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026