Status:

UNKNOWN

Cervical Erector Spinae Block Versus Interscalene Block for Shoulder Surgery

Lead Sponsor:

Ataturk University

Conditions:

Pain, Acute

Opioid Use

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

Severe pain after arthroscopic surgery is a common experience for the patients . Different regional anesthetic technique has been applicated for postoperative pain relief . The main goal of regional a...

Detailed Description

This study has been designed as a prospective, randomized and single-blind trial. Local ethics committee of Ataturk University has approved the study (B.30.2.ATA.0.01.00/142). After obtaining the pati...

Eligibility Criteria

Inclusion

  • Age between 18-80
  • ASA I-III
  • Eligible for regional anesthesia
  • Unilateral shoulder surgery

Exclusion

  • The patients who have clotting disorder
  • Contra-endication for regional anesthesia
  • Infection on the injection site
  • Chronic opioid usage
  • Previous same side shoulder surgery
  • Severe COPD
  • Diaphragmatic paralysis
  • BMI 35 or over

Key Trial Info

Start Date :

October 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2022

Estimated Enrollment :

94 Patients enrolled

Trial Details

Trial ID

NCT04435236

Start Date

October 1 2021

End Date

May 1 2022

Last Update

June 22 2021

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Cervical Erector Spinae Block Versus Interscalene Block for Shoulder Surgery | DecenTrialz