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Clinical Trials/NCT02287142
NCT02287142
Completed
Not Applicable

Evaluation of Supraclavicular, Suprascapular, and Interscalene Nerve Blocks for Outpatient Shoulder Surgery

Benaroya Research Institute1 site in 1 country189 target enrollmentOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Benaroya Research Institute
Enrollment
189
Locations
1
Primary Endpoint
Pain
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The aim of this study is to assess analgesic efficacy of a supraclavicular nerve block, suprascapular nerve block, or interscalene nerve block in a population undergoing shoulder arthroscopy with rotator cuff repair. The investigators hypothesize that subjects from all three arms will receive equal analgesia since these blocks are routinely performed to treat post-operative pain after shoulder surgery.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
November 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

David Auyong

Anesthesiologist

Benaroya Research Institute

Eligibility Criteria

Inclusion Criteria

  • Unilateral total shoulder arthroscopy for rotator cuff surgery ASA physical status I-III, \>18 years old, Non-pregnant, Consent to participate in the study

Exclusion Criteria

  • Refusal to participate, \< 18 years old, Chronic opioid use, Localized infection, Pregnancy or lactating, Pre-existing coagulopathy, Allergy to ultrasound gel or local anesthetics, Diaphragmatic dysfunction

Outcomes

Primary Outcomes

Pain

Time Frame: Same day, 1 hour after arrival in the post-anesthesia care unit after surgery

NRS Pain Scale

Secondary Outcomes

  • Lung function(Same day, 1 hour after arrival in the post-anesthesia care unit after surgery)
  • Sensory and Motor Function(Same day, 1 hour after arrival in the post-anesthesia care unit after surgery)
  • Diaphragmatic excursion(Same day, 1 hour after arrival in the post-anesthesia care unit after surgery)

Study Sites (1)

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