Quadratus Lumborum Block Versus Erector Spinae Block in Laparoscopic Cholecystectomy

Not Applicable

Completed

• Conditions: Postoperative Analgesia

• Registration Number: NCT04689633
• Lead Sponsor: Minia University

Brief Summary

The patients were randomly allocated into 3 parallel groups of 20 patients in each group by using computer generated tables. group(Q):received bilateral sonar-guided quadratus lumborum bolck using 20 ml bupivacaine 0.25%on each side.group(E): received bilateral ultrasound-guided erector spinae block using 20 ml bupivaciane 0.25%on each side. group(C):didn't received any block

Detailed Description

on arrival to the operative room all patients were monitored with standared monitoring. then IV cannula were inserted. preoxygenation with 100% oxygen and induction of GA by 1mic/kg fentanyl and 2 mg/kg of 1%propofol. endotracheal intubation was facilitated by 0.5mg/kg of atracurium. isoflurane 1-2% with oxygen was used for anesthetic maintenance and 0.15 mg/kg intermittent doses of atracurium to maintain adequate muscle relaxation. ventilation was controlled to maintain end tidal CO2 at 35-40 mmHg and SaO2 between 95-100. after stabilization of the patient's hemodynamics and before surgical incision, quadratus lumborum and erector Spinae block were performed according to patient's group by the same anesthetist with the patient in lateral or prone position respectively.

Study Timeline

• Status Verified: 2018-12
• Study Start: 2019-04-15
• Primary Completion: 2019-12-15
• Study Completion: 2020-01-15
• Study First Submitted: 2020-12-29
• Study First Submitted QC: 2020-12-29
• Study First Posted: 2020-12-30
• Last Update Submitted: 2021-03-02
• Last Update Posted: 2021-03-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• American society of anesthesiologists(ASA) physical status1and2 scheduled for elective cholecystectomy under general anesthesia

Exclusion Criteria

• Allergy to studed drugs
• morbid obesity
• patient refusal
• infection at the side of the bolck
• emergency laparoscopic cholecystectomy
• if laparoscopic procedure converted to open

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
time of first postoperative analgesic request	24 hours	first time that patient need analgesia and visual analogue scale more than 3

Trial Locations

Locations (1)

Faculty of Medicine; 🇪🇬 Minya, Egypt