Erector Spinae Plane Block in Renal Transplantation Donors

Not Applicable

Completed

• Conditions: Renal Transplantation; Erector Spinae Plane Block; Laparoscopic Nephrectomy

• Registration Number: NCT04863716
• Lead Sponsor: Koc University Hospital

Brief Summary

Erector Spina Plan Block (ESPB) is a relatively new, easy-to-apply and safe regional anesthesia technique used to provide postoperative analgesia in various surgeries. Studies showing the clinical benefits of Erector Spina Plan block in renal transplantation surgery are limited to case reports. In this study, the effect of Erector Spina Plan Block on opioid consumption in postoperative period on donor patients who will undergo laparoscopic nephrectomy in renal transplantation surgery will be examined prospectively.

The aim of the study is to provide analgesia to donor patients using less opioids by Erector Spina Plan Block and provide enhanced recovery.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-04-20
• Study First Submitted QC: 2021-04-26
• Study Start: 2021-04-28
• Study First Posted: 2021-04-28
• Primary Completion: 2022-04-10
• Study Completion: 2022-04-14
• Status Verified: 2022-09
• Last Update Submitted: 2022-09-20
• Last Update Posted: 2022-09-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 52

Inclusion Criteria

• Donor patients scheduled for elective nephrectomy in renal transplantation surgery
• ASA I-II
• Patients who are aged between 18-75

Exclusion Criteria

• Skin infection at the Erector Spina Plan Block area
• Coagulation disorder or using anticoagulant drugs
• End-stage organ and system failure
• Severe pulmonary and/or cardiovascular problems
• Substance addiction or known psychiatric or mental problems
• Chronic painkiller usage

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Fentanyl consumption	Postoperative 24 hours	The amount of fentanyl required by the patient and given by the device will be recorded for the first 24 hours.

Secondary Outcome Measures

Name	Time	Method
Visual Analog Scale	Postoperative 24 hours	Pain of patients will be evaluated and recorded according to the Visual Analog Scale.
Modified Aldrete Score	Postoperative 1 hour	Modified Aldrete Score will be used in patient recovery, and scores will be recorded at 5 minute intervals.

Trial Locations

Locations (1)

Koç University Hospital; 🇹🇷 Istanbul, Zeytinburnu, Turkey