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Clinical Trials/NCT04845711
NCT04845711UnknownNot Applicable

Ultrasound Guided Erector Spinae Plane Block Versus Quadratus Lumborum Block for Postoperative Analgesia in Laparoscopic Cholecystectomy Surgeries: A Randomized Controlled Trial

Tanta University0 sites60 target enrollmentStarted: May 1, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
60
Primary Endpoint
The degree of postoperative pain in the first 24 hours post-operative

Study Overview

Brief Summary

The aim of this study is to compare between the efficacy of ultrasound guided erector spinae plane block and ultrasound guided quadratus lumborum block in managing acute postoperative pain in patients undergoing laparoscopic cholecystectomy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Masking Description

Patients and medical personnel collecting data and conducting follow-up will be blinded to the group of the patient. All blocks will be performed by one anesthesiologist who will not participate in data collection or analysis.

Eligibility Criteria

Ages
21 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • aged 21-65 years
  • both genders
  • American Society of Anesthesiology (ASA) class I-II
  • Undergoing elective laparoscopic cholecystectomy

Exclusion Criteria

  • Patient refusal.
  • Coagulopathy.
  • History of allergy to local anaesthetic.
  • History of liver or renal pathology affecting drug elimination
  • Mental dysfunction or cognitive disorders.
  • Use of medication such as gabapentin-pregabalin that could affect pain perception.
  • Body Mass Index > 40 kg/m2.

Outcomes

Primary Outcomes

The degree of postoperative pain in the first 24 hours post-operative

Time Frame: first 24 hours post-operative

Postoperative pain will be assessed by the numerical rating scale (NRS); 0 no pain while 10 is the maximum pain) after discharge to the ward ,and at 6, 12, 18, 24 hours.

Secondary Outcomes

  • Time to first analgesic requirement(first 24 hours post-operative)
  • Total dose of intraoperative consumption of fentanyl(intraoperative)
  • Total dose of rescue analgesia in the first 24hr postoperative(first 24 hours post-operative)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mai Elsaid Hamada

Resident of Anesthesiology, Surgical Intensive Care and Pain Medicine

Tanta University

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