Skip to main content
Clinical Trials/NCT05533710
NCT05533710
Recruiting
Not Applicable

Comparative Study Between Bilateral Ultrasound-Guided Erector Spinae Plane Block Versus Bilateral Ultrasound-Guided Transversus Abdominis Plane Block on Postoperative Analgesia After Total Abdominal Hysterectomy

Ain Shams University1 site in 1 country40 target enrollmentAugust 28, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Uterine Diseases
Sponsor
Ain Shams University
Enrollment
40
Locations
1
Primary Endpoint
Total morphine consumption
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

This study aims to compare the ultrasound-guided bilateral erector spinae block versus the ultrasound-guided bilateral transversus abdominis plane block on postoperative analgesia after total abdominal hysterectomy.

Registry
clinicaltrials.gov
Start Date
August 28, 2021
End Date
August 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Israa Ihab Abdel Aziz

assistant lecturer

Ain Shams University

Eligibility Criteria

Inclusion Criteria

  • Patients American Society of Anesthesiologists physical status (ASA) I and II.
  • Female sex.
  • Age between 40 to 60 years old.
  • Scheduled for elective total abdominal hysterectomy surgeries.

Exclusion Criteria

  • Patient's refusal.
  • Patients who received long-acting opioids preoperatively.
  • Patients with bleeding disorders and coagulopathy.
  • Infection at the injection site.
  • Allergy to local anesthetics.
  • Patients with significant cognitive dysfunction.
  • Patients with diabetic neuropathy.
  • Patients with uncontrolled hypertension or diabetes.
  • Patients with advanced cardiac, respiratory, hepatic or renal disease.
  • Patients with viral hepatitis or HIV.

Outcomes

Primary Outcomes

Total morphine consumption

Time Frame: 24 hours postoperative

Compare postoperative pain intensity using the total amount of morphine consumption in the first 24 hours after the operation, and the time for first call rescue analgesia

Visual Analog Scale Score

Time Frame: 24 hours postoperative

Compare postoperative pain intensity using VAS score in the first 24 hours after the operation.The VAS score is a 10-cm line labeled with "worst pain imaginable" on the right border, and "no pain" on the left border (ranging from 0 by indicating no pain to 10 indicating extreme pain).

The time for first call rescue analgesia

Time Frame: 24 hours postoperative

the time for first call rescue analgesia

Secondary Outcomes

  • Patient satisfaction(24 hours postoperative)
  • Recognize the adverse effects(24 hours postoperative)

Study Sites (1)

Loading locations...

Similar Trials