Pericapsular Nerve Group Block for Total Hip Arthroplasty

Postoperative Pain Clinical Trial

Official title: Efficacy of Pericapsular Nerve Group Block After Total Hip Arthroplasty Surgery

Status Completed

Clinical Trial Summary

Controlling pain after hip replacement surgery improves comfort and partient satisfaction. Pain after hip replacement has traditionally been managed using systemic pain medications including acetaminophen and non-steroidal anti-inflammatory drugs. A recent Cochrane review demonstrated that compared to systemic analgesia alone, peripheral nerve blocks reduce postoperative pain with moderate-quality evidence. Pericapsular Nerve Group block is a new technique allowing local anesthetic diffusion to femoral, obturator and accessory obturator nerves and providing a good analgesic effect for hip fracture surgery. Investigators hypothesized that the PENG block could be an interesting alternative to systemic analgesiscs for pain control after total hip replacement.

Clinical Trial Description

The aim of the study was to evaluate the efficacy of the PENG block for intra and postoperative pain control in total hip arthroplasty.

it was a monocentric, randomized, controlled and double blind study. Patients scheduled for primary THA with lateral approach under general anesthesia.

Premedication with IV midazolam 1 to 2 mg on arrival to operating theatre. general anesthesia was conducted using fentanyl, propofol and cisatracurium for induction and isoflurane for maintanance patients were randomized using a random table in two groups:

• PENG Block group (PG) who received 2 mg.kg-1Ropivacaine in 40 ml of saline.

• Placebo group (SG) who received 40 ml of saline.

Postoperative analgesia started before extubation of the patient, with:

• IV paracetamol 1g/6h in Day1 and oral paracetamol 1g/8h for 6 days.

• non steroidal anti inflammatory drugs with IM piroxicam 20 mg on day one (at the end of surgery) and oral diclofenac 50 mg/12h for 3 days.

• Morphine PCA for day 1 (24 H) and oral tramadol 50 mg/12h from day 2 to day 6. ;

Related Conditions & MeSH terms

• Hip Arthropathy
• Joint Diseases
• Pain, Postoperative
• Postoperative Pain

• NCT number: NCT04295408
• Study type: Interventional
• Source: University Tunis El Manar
• Status: Completed
• Phase: N/A
• Start date: April 30, 2020
• Completion date: December 31, 2021