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Clinical Trials/NCT05141955
NCT05141955
Completed
N/A

A Randomized Controlled Trial for Postoperative Analgesia in Patients Undergoing Laparoscopic Sleeve Gastrectomy: Ultrasound Guided Erector Spinae Plane Block Versus Quadratus Lumborum Block

Ain Shams University1 site in 1 country120 target enrollmentDecember 15, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Post Operative Pain
Sponsor
Ain Shams University
Enrollment
120
Locations
1
Primary Endpoint
Time to first requested rescue analgesia(Minutes)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Postoperative pain control is a significant challenge in medical practice. Inadequate pain control could decrease patient's satisfaction, delay postoperative ambulation, increase the incidence of pulmonary and cardiac complications and cause the development of chronic postoperative pain. Laparoscopic surgical techniques could decrease postoperative pain and opioid consumption.

The addition of regional techniques to general anesthesia showed better pain management and less consumption of opioids compared to the traditional techniques.

The aim of this study is to compare the effectiveness of ultrasound guided erector spinae plane block versus quadratus lumborum block regarding postoperative analgesia in patients undergoing laparoscopic sleeve gastrectomy.

Registry
clinicaltrials.gov
Start Date
December 15, 2021
End Date
June 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr.Ibrahim Mamdouh Esmat

Assistant Professor of Anesthesia and Intensive Care Department, Faculty of Medicine, Ain- shams University, Cairo, Egypt.

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • Patients with free medical history or controlled hypertension and/ or diabetes scheduled for elective laparoscopic sleeve gastrectomy.
  • BMI \> 35 kg/ m2

Exclusion Criteria

  • Patients unfit for surgery or refuse to sign the consent of regional block.
  • Patients with known coagulation defects.
  • Patients with known hypersensitivity to bupivacaine.
  • Patients with infection at the site of injection.
  • Conversion of laparoscopic surgery to laparotomy

Outcomes

Primary Outcomes

Time to first requested rescue analgesia(Minutes)

Time Frame: 24 hours postoperatively

Time to first requested rescue analgesia(Minutes)

Study Sites (1)

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