Ultrasound Guided Erector Spinae Plane Block Versus Quadratus Lumborum Block in Laparoscopic Cholecystectomy

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-01

Study Completion Date

2021-11-01

Brief Summary

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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.

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Detailed Description

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Conditions

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Laparoscopic Cholecystectomy Postoperative Analgesia Erector Spinae Plane Block Quadratus Lumborum Block

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

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.

Study Groups

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Control group

patients will receive general anesthesia only.

Group Type PLACEBO_COMPARATOR

Control group

Intervention Type OTHER

patients will receive general anesthesia only.

Erector spinae plane block group

patients will receive general anesthesia and bilateral ultrasound guided erector spinae plane block (20ml Bupivacaine 0.25%)

Group Type EXPERIMENTAL

Erector spinae plane block group

Intervention Type PROCEDURE

patients will receive general anesthesia and bilateral ultrasound guided erector spinae plane block (20ml Bupivacaine 0.25%)

Quadratus lumborum block group

patients will receive general anesthesia and bilateral ultrasound guided quadratus lumborum block (20 ml Bupivacaine 0.25%)

Group Type EXPERIMENTAL

Quadratus lumborum block group

Intervention Type PROCEDURE

patients will receive general anesthesia and bilateral ultrasound guided quadratus lumborum block (20 ml Bupivacaine 0.25%)

Interventions

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Control group

patients will receive general anesthesia only.

Intervention Type OTHER

Erector spinae plane block group

patients will receive general anesthesia and bilateral ultrasound guided erector spinae plane block (20ml Bupivacaine 0.25%)

Intervention Type PROCEDURE

Quadratus lumborum block group

patients will receive general anesthesia and bilateral ultrasound guided quadratus lumborum block (20 ml Bupivacaine 0.25%)

Intervention Type PROCEDURE

Other Intervention Names

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Group C group ESPB group QLB

Eligibility Criteria

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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.

Minimum Eligible Age

21 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No