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
NA
140 participants
INTERVENTIONAL
2015-07-31
2016-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Normal pre-operative education
• Control group received normal pre-operative education regarding surgery
No interventions assigned to this group
Opioid usage education
• The study group received formal education detailing recommended post-operative opioid usage, side effects, dependence, and addiction
Formal education regarding opioid usage
Participannts watched a 2 minute video and were given educational materials
Interventions
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Formal education regarding opioid usage
Participannts watched a 2 minute video and were given educational materials
Eligibility Criteria
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Inclusion Criteria
* clinically indicated for an arthroscopic rotator cuff repair
Exclusion Criteria
* allergic or sensitivity to the study medication
* history of gastrointestinal issues
* any evidence of glenohumeral arthritis
* inability to consent
18 Years
ALL
No
Sponsors
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Rothman Institute Orthopaedics
OTHER
Responsible Party
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Other Identifiers
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2017Abb
Identifier Type: -
Identifier Source: org_study_id
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