Bilateral vs. Unilateral Erector Spinae Plane Block

Not Applicable

Completed

• Conditions: Postoperative Pain; Cholecystitis; Gallstone
• Interventions: Procedure: Bilateral ESP Block; Procedure: Unilateral ESP Block; Device: Intravenous Morphine patient controlled analgesia device

• Registration Number: NCT03781687
• Lead Sponsor: Kocaeli University

Brief Summary

The importance of multimodal analgesia for postoperative pain management is well known and regional anesthesia techniques are commonly prefferred to provide better analgesia. Erector spinae plane block (ESB) is a new defined and effective regional anesthesia technique. But two injections can be unconfortable for some patients. With this study, we aimed to compare the analgesia effect of bilateral and unilateral ESP block for laparoscopic cholecystectomy.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2018-12-18
• Study First Submitted QC: 2018-12-18
• Study First Posted: 2018-12-20
• Study Start: 2019-01-02
• Primary Completion: 2019-06-28
• Study Completion: 2019-06-29
• Status Verified: 2019-11
• Last Update Submitted: 2019-11-21
• Last Update Posted: 2019-11-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

• ASA I-II patients
• Pateints undergoing elective laparoscopic cholecystectomy

Exclusion Criteria

• obesity (body mass index >35 kg/m2)
• infection of the skin at the site of needle puncture area
• patients with known allergies to any of the study drugs
• coagulopathy
• recent use of analgesic drugs

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Bilateral	Intravenous Morphine patient controlled analgesia device	Bilateral ESP block will be performed
Bilateral	Bilateral ESP Block	Bilateral ESP block will be performed
Unilateral	Intravenous Morphine patient controlled analgesia device	Unilateral ESP block will be performed
Unilateral	Unilateral ESP Block	Unilateral ESP block will be performed

Primary Outcome Measures

Name	Time	Method
Morphine consumption	preoperative 24th hour	Morphine consumption will be recorded

Secondary Outcome Measures

Name	Time	Method
Numeric Rating Scale	postoperative 24th hour	A NRS involves asking the patient to rate his or her pain from 0 to 10 (11 point scale) with the understanding that 0 is equal to no pain and 10 is equal to worst possible pain.

Trial Locations

Locations (1)

Kocaeli University Hospital; 🇹🇷 İzmit, Kocaeli, Turkey