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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COMPLETED
36 participants
OBSERVATIONAL
2018-06-13
2019-07-01
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
Study Groups
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Arthroscopic Rotator Cuff Repair
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* clinically indicated for an Arthroscopic Rotator Cuff Repair (ARCR)
Exclusion Criteria
* allergic or sensitivity to the study medication
* intolerance to pain protocol
* history of gastrointestinal issues
* renal disease
* any evidence of glenohumeral arthritis
18 Years
ALL
No
Sponsors
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Rothman Institute Orthopaedics
OTHER
Responsible Party
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Locations
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Rothman Institute
Philadelphia, Pennsylvania, United States
Countries
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Other Identifiers
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2018LAustin
Identifier Type: -
Identifier Source: org_study_id
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