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
252 participants
OBSERVATIONAL
2013-07-31
2017-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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pre-MP3
before implementation of the multimodal analgesia protocol
No interventions assigned to this group
post-MP3
after implementation of the multimodal analgesia protocol
multimodal perioperative pain protocol (MP3)
administration of gabapentionoid, acetaminophen, non steroidal anti-inflammatory drugs around the clock in addition to the peripheral nerve block offered before surgery
Interventions
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multimodal perioperative pain protocol (MP3)
administration of gabapentionoid, acetaminophen, non steroidal anti-inflammatory drugs around the clock in addition to the peripheral nerve block offered before surgery
Eligibility Criteria
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Inclusion Criteria
* Age 18-80
* Speaks and understands the English language
* Have a phone number
* Scheduled for shoulder arthroscopy
Exclusion Criteria
* Individuals outside of age range
* Pregnant women
* Persons under the jurisdiction of the Department of Corrections
18 Years
80 Years
ALL
No
Sponsors
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University of Pennsylvania
OTHER
Responsible Party
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Nabil Elkassabany
Assistant Professor
References
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Elkassabany NM, Wang A, Ochroch J, Mattera M, Liu J, Kuntz A. Improved Quality of Recovery from Ambulatory Shoulder Surgery After Implementation of a Multimodal Perioperative Pain Management Protocol. Pain Med. 2019 May 1;20(5):1012-1019. doi: 10.1093/pm/pny152.
Other Identifiers
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818312
Identifier Type: -
Identifier Source: org_study_id
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