Variation in Humeral Head Bone Marrow Characteristics with Rotator Cuff Repair Healing
NCT ID: NCT05106088
Last Updated: 2025-03-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
50 participants
OBSERVATIONAL
2021-11-22
2026-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* 18-75 years
* 1-5 cm full thickness tear of the supraspinatus and/or infraspinatus tendon(s) that is fully reparable by double row technique as confirmed at surgery
Exclusion Criteria
* symptomatic cervical spine disease
* a frozen shoulder-- defined as a loss of passive range of motion (ROM) of more than 20° in any plane compared to the contralateral shoulder
* advanced (grade 3 or 4) glenohumeral arthritis
* worker's compensation cases
* isolated subscapularis tears.
18 Years
75 Years
ALL
Yes
Sponsors
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The Cleveland Clinic
OTHER
Responsible Party
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Kathleen Derwin, PhD
Associate Staff Scientist
Principal Investigators
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Kathleen Derwin, PhD
Role: PRINCIPAL_INVESTIGATOR
The Cleveland Clinic
Locations
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Cleveland Clinic
Cleveland, Ohio, United States
Countries
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Other Identifiers
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21-811
Identifier Type: -
Identifier Source: org_study_id
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