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Comparison of retear rate after rotator cuff repair according to injection of bone marrow aspirate concentrate

Not Applicable
Conditions
Diseases of the musculoskeletal system and connective tissue
Registration Number
KCT0007825
Lead Sponsor
Seoul National University Bundang Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
144
Inclusion Criteria

(1) Among patients aged 19 or older, patients who will undergo surgery due to rotator cuff tear at participating institutions (Seoul National University Bundang Hospital, Seoul National University Hospital, and Konkuk University Hospital) in this study.
(2) Patients with rotator cuff tear size more than 2.5 cm on preoperative magnetic resonance imaging.

Exclusion Criteria

(1) Patients with the history of surgery on the rotator cuff on the ipsilateral shoulder
(2) Patients with the history of trauma on the ipsilateral shoulder
(3) Patients with the history of infection (or surgery due to infection) on the ipsilateral shoulder
(4) Patients with the history of fracture (or surgery due to infection) on the ipsilateral shoulder
(5) Patients with the history of proliferative treatment or treatment with corticosteroid, atelocollagen, or polydeoxyribonucleotide on the ipsilateral shoulder within three months of surgery
(6) Patients who decide not to participate in this study after sufficient explanation from the participating researchers
(7) If additional operation will be done due to the suture anchor breakage or pull-out during the surgery, such as bone cement filling or buddy anchor insertion.

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Retear rate
Secondary Outcome Measures
NameTimeMethod
Functional score{American Shoulder and Elbow Surgeons Score (ASES), Simple shoulder test (SST), Constant-Murley Score (CMS)};Pain VAS;Range of motion (Forward flexion, external rotation, and internal rotation)
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