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Multimodal Analgesia After Shoulder Arthroscopy

NCT03427775 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 252

Last updated 2019-07-18

No results posted yet for this study

Summary

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.

Conditions

  • Analgesia
  • Arthroscopy
  • Shoulder Joint

Interventions

COMBINATION_PRODUCT

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

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2016-04-30
Completion
2017-07-31
FDA Drug
Yes

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03427775 on ClinicalTrials.gov