Multimodal Analgesia After Shoulder Arthroscopy

NCT ID: NCT03427775

Last Updated: 2019-07-18

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

252 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-07-31

Study Completion Date

2017-07-31

Brief Summary

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This proposal aims to measure the quality of recovery and quality of pain management after shoulder surgery before and after implementation of a multimodal pain protocol.

Detailed Description

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Pain management after shoulder surgery remains to be a major challenge. Reliance on a single agent (most commonly opioids) results in increased incidence of side effects. Multimodal pain management refers to the use of multiple drugs that target different components of pain pathway.

Conditions

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Analgesia Arthroscopy Shoulder Joint

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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)

Intervention Type COMBINATION_PRODUCT

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

Intervention Type COMBINATION_PRODUCT

Eligibility Criteria

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Inclusion Criteria

* Adult patients
* Age 18-80
* Speaks and understands the English language
* Have a phone number
* Scheduled for shoulder arthroscopy

Exclusion Criteria

* Inability to read or speak English
* Individuals outside of age range
* Pregnant women
* Persons under the jurisdiction of the Department of Corrections
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Pennsylvania

OTHER

Sponsor Role lead

Responsible Party

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Nabil Elkassabany

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

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.

Reference Type DERIVED
PMID: 30113685 (View on PubMed)

Other Identifiers

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818312

Identifier Type: -

Identifier Source: org_study_id

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