Erector Spinae Plane Block for Postoperative Analgesia for Laparoscopic Cholecystectomy

Not Applicable

Completed

• Conditions: Postoperative Pain
• Interventions: Other: erector spinae plane block; Device: Intravenous morphine patient controlled analgesia device

• Registration Number: NCT03420703
• Lead Sponsor: Kocaeli University

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 application of this blockade into practice at the clinic. Main purpose of this study is to evaluate the analgesic effect of ultrasound guided erector spinae block in laparoscopic cholecystectomy.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2018-01-29
• Study First Submitted QC: 2018-01-29
• Study First Posted: 2018-02-05
• Study Start: 2018-02-24
• Primary Completion: 2018-04-18
• Study Completion: 2018-04-18
• Status Verified: 2018-06
• Last Update Submitted: 2018-06-13
• Last Update Posted: 2018-06-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

• 25 - 75 years of age
• ASA I - II
• Undergoing elective laparoscopic cholecystectomy

Exclusion Criteria

• obesity
• ASA III - IV
• 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
Block group	erector spinae plane block	Erector espine plane block will be administrated to this group. An intravenous patient controlled analgesia device will be given to the patients postoperatively
Block group	Intravenous morphine patient controlled analgesia device	Erector espine plane block will be administrated to this group. An intravenous patient controlled analgesia device will be given to the patients postoperatively
control group	Intravenous morphine patient controlled analgesia device	An intravenous patient controlled analgesia device will be given to the patients postoperatively

Primary Outcome Measures

Name	Time	Method
24h morphine consumption	for postoperative 24 hour	morphine consumptions for both group will be recorded

Secondary Outcome Measures

Name	Time	Method
Pain	24h	Numeric rating scales were recorded
Postoperative nausea and vomiting	24 hour	PONV after surgery was questioned

Trial Locations

Locations (1)

Kocaeli University Hospital; 🇹🇷 İzmit, Kocaeli, Turkey