Erector Spinae Plane Block Versus Quadratus Lumborum Block For Postoperative Analgesia After Abdominal Hysterectomy

Anesthesia Clinical Trial

Official title:

Erector Spinae Plane Block Versus Quadratus Lumborum Block For Postoperative Analgesia After Abdominal Hysterectomy; A Randomized Comparative Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05541588
• Other study ID #: ASUKH1
• Status: Recruiting
• Phase: N/A
• Start date: July 7, 2022
• Est. completion date: January 2023

Study information

• Verified date: September 2022
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to compare the analgesic efficacy of erector spinae plane block and quadratus lumborum block after abdominal hysterectomy surgery and postoperative opioid consumption.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 64
• Est. completion date: January 2023
• Est. primary completion date: January 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Patients with American Society of Anesthesiologists (ASA) physical status 1-3.

• scheduled for abdominal hysterectomy surgery.

Exclusion Criteria:

• History of allergy to the medications used in the study.

• Contraindication to regional anesthesia as coagulopathy, local infection.

• Severe hepatic impairment (child C).

• Sever Renal dysfunction (creatinine clearance < 30).

• Psychiatric or mental disorder affecting patient ability to interpret VAS score.

• Body mass index (BMI) = 40 or = 18 kg/m2.

• ASA IV.

• Patient refusal.

Related Conditions & MeSH terms

• Anesthesia

Intervention

Procedure:
• peripheral nerve block
ultrasound guided nerve block

Locations

Country	Name	City	State
Egypt	Ain Shams univerisity	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incidence of complications	postoperative nausea and vomiting(PONV), hematoma, local anaesthetic toxicity (LAT)	24 hours
Primary	Post-operative pain	Post-operative pain severity assessed by visual analog scale (VAS) (range from 0-10., 0 no pain, 10 worst pain ).	24 hours
Secondary	Cumulative post-operative opioid consumption	opioid consumption	24 hours
Secondary	The onset of 1st analgesic request	time needed for 1st request of rescue analgesia	24 hours