Comparing Pericapsular Nerve Group Block with Lumbar Erector Spinae Plain Block in Total Hip Arthroplasty Surgery

Not Applicable

Completed

• Conditions: Postoperative Pain; Total Hip Arthroplasty

• Registration Number: NCT06059339
• Lead Sponsor: Marmara University

Brief Summary

Total hip arthroplasty is a common surgical procedure aiming to improve mobility and quality of life in patients suffering from hip pain. Despite being a frequently performed procedure, there is high variability in the peri-operative anaesthetic and analgesic management for total hip arthroplasty.

Beyond the immediate postoperative period, regional anesthesia and analgesia can have potentially beneficial effects on long-term outcomes, especially on postoperative pain, functional rehabilitation and morbidity .

The primary implication of this study is to compare postoperative opioid consumption of patients' after total hip arthroplasty using pericapsular nerve group (PENG) block with lumbar erector spinae plain block.

Detailed Description

Total hip arthroplasty is a common surgical procedure aiming to improve mobility and quality of life in patients suffering from hip pain. Despite being a frequently performed procedure, there is high variability in the peri-operative anaesthetic and analgesic management for total hip arthroplasty.

Beyond the immediate postoperative period, regional anesthesia and analgesia can have potentially beneficial effects on long-term outcomes, especially on postoperative pain, functional rehabilitation and morbidity .

The primary implication of this study is to compare postoperative opioid consumption of patients' after total hip arthroplasty using pericapsular nerve group (PENG) block with lumbar erector spinae plain block.

Study Timeline

• Study First Submitted: 2023-04-04
• Study Start: 2023-04-22
• Study First Submitted QC: 2023-09-27
• Study First Posted: 2023-09-28
• Status Verified: 2024-07
• Primary Completion: 2024-07-31
• Study Completion: 2024-07-31
• Last Update Submitted: 2025-01-08
• Last Update Posted: 2025-01-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

• Patients over 18 years old, undergoing total hip arthroplasty surgery

Exclusion Criteria

• Patients with solid organ dysfunction, chronic opioid or corticosteroid use, bleeding diathesis, patients receiving inpatient medication, patients with psychiatric disorders and patients who cannot be contacted after surgery.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Opioid Consumption	24 Hours	Comparing opioid consumption via Patient Controlled Analgesia (PCA) device; 1 mg/ ml morphine, 10 minutes lock out

Secondary Outcome Measures

Name	Time	Method
Pain Scores	48 Hours	Numeric Rating Scale: (0 to 10: worse pain:10 no pain:0)
rescue analgesia	48 hours	tramadol 1.5 mg/kg if NRS\>4.

Trial Locations

Locations (1)

Marmara University; 🇹🇷 Istanbul, Turkey