A Randomized Comparison between Infraclavicular/Suprascapular and Axillary/Suprascapular Nerve Blocks for Arthroscopic Rotator Cuff Repair

Phase 2

Completed

• Conditions: Infraclavicular brachial plexus blockSuprascapular nerve blockAxillary nerve blockArthroscopic rotator cuff repair; Analgesia; Nerve Block; Arthroscopy

• Registration Number: TCTR20151126002
• Lead Sponsor: one

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-11-26
• Study Completion: 2016-05-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

- patients undergoing arthroscopic rotator cuff repair
- American Society of Anesthesiologists classification 1-3
- body mass index between 18 and 30

Exclusion Criteria

- adults who are unable to give their own consent
-pre-existing neuropathy
-coagulopathy
-renal failure or hepatic failure
-allergy to local anesthetics (LAs)
-pregnancy
-prior surgery in the infraclavicular region, shoulder or suprascapular fossa
- chronic pain syndromes requiring opioid intake at home

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Proportion of patients reporting moderate to severe postoperative pain at 30 minutes in recovery room Pain score (Numeric rating scale)

Secondary Outcome Measures

Name	Time	Method
Postoperative pain score at 24 hours after surgery Pain score (Numeric rating scale),Post-operative opioid consumption at 24 hours after surgery Total amount of morphine,Intra-operative opioid consumption at the end of surgery Total amount of fentanyl,Patient's satisfaction at 24 hours after surgery a 0-10 scale,Hemidiaphragmatic paralysis in recovery room Ultrasonography