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Clinical Trials/NCT03869801
NCT03869801
Completed
Not Applicable

Comparison of Ultrasound Guided Bilateral Erector Spinae Plane Block and Quadratus Lumborum Block in Laparoscopic Cholecystectomy

Maltepe University3 sites in 1 country80 target enrollmentMarch 15, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Maltepe University
Enrollment
80
Locations
3
Primary Endpoint
analgesic consumption
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Erector Spinae Plane Block is a newly defined regional anesthesia technique. Its use for many indications has been identified by case reports in the literature. As the investigators have considered that erector spinae plane block could be efficacious for providing postoperative analgesia in laparoscopic cholecystectomy, the investigators have implemented the application of this blockade into practice at the clinic.Quadratus Lumborum block (QLB) type 2 is another regional anesthesia technic used for postoperative analgesia in laparoscopic cholecystectomy. Main purpose of this study is to compare the analgesic effect of ultrasound-guided erector spinae block and QLB in laparoscopic cholecystectomy.

Registry
clinicaltrials.gov
Start Date
March 15, 2019
End Date
May 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Asst. Prof. Serkan Tulgar, M.D.

associate professor in anesthesiology

Maltepe University

Eligibility Criteria

Inclusion Criteria

  • Elective laparoscopic Cholecystectomy, ASA status 1-2

Exclusion Criteria

  • Patient refusal Contraindications to regional anesthesia Known allergy to local anesthetics Bleeding diathesis Use of any anti-coagulants Inability to provide informed consent Severe kidney or liver disease Inability to operate PCA system Patient with psychiatric disorders

Outcomes

Primary Outcomes

analgesic consumption

Time Frame: 24 hours

opioid consumption in Patient Controlled Analgesia device

Secondary Outcomes

  • NRS scores(24 hours)

Study Sites (3)

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