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Clinical Trials/NCT05646667
NCT05646667
Completed
Not Applicable

Interscalene Block Alone Versus Interscalene Block With Erector Spinae Plane Block for Shoulder Arthroscopy Anesthesia: A Randomized Controlled Trial

Tanta University1 site in 1 country50 target enrollmentDecember 15, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Interscalene Block
Sponsor
Tanta University
Enrollment
50
Locations
1
Primary Endpoint
Intraoperative fentanyl consumption
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to compare the effectiveness of interscalene brachial plexus block alone versus interscalene brachial plexus block +Erector spinae plane block in anesthesia for shoulder arthroscopy.

Detailed Description

Regional anesthetic techniques can control pain effectively, both at rest and on movement, allowing earlier mobilization without the adverse effects of opioids . Among the various types of regional anesthetic techniques, the interscalene brachial plexus block is a gold standard used nerve block technique for postoperative analgesia in patients undergoing shoulder surgery, as it has consistently been shown to significantly control.

Registry
clinicaltrials.gov
Start Date
December 15, 2022
End Date
February 15, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Islam Morsy

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine

Tanta University

Eligibility Criteria

Inclusion Criteria

  • Aged 18-65 years
  • Both genders,
  • BMI \< 40 kg/m2
  • American Society of Anesthesiologists (ASA) physical status I-II
  • Scheduled for elective shoulder arthroscopy.

Exclusion Criteria

  • Known allergy to local anesthetics,
  • allergy to all opioid medications, diagnostic shoulder arthroscopic procedures,
  • patients with chronic opioids,
  • patients who converted to general anesthesia use and coagulopathy

Outcomes

Primary Outcomes

Intraoperative fentanyl consumption

Time Frame: Intraoperative up to 4 hours

If the patient complains of pain during surgery, fentanyl will be administered 1 µg/kg IV increments.

Secondary Outcomes

  • Amount of 24hrs postoperative rescue analgesic consumption(24 hours postoperatively)
  • Degree of pain by Numerical pain rating scale(24 hours postoperatively)
  • Time to first request of rescue analgesia.(24 hours postoperatively)

Study Sites (1)

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