Deep Posterior Post Gluteal Compartment Block in Total Hip Arthroplasty: Feasability and Safety (ANATH)

Quincy Anesthésie

Status: Not yet enrolling

Conditions: Total Hip Arthroplasty

Treatments: Procedure: Deep posterior post gluteal nerve block

Study type: Interventional

Funder types: NETWORK

Identifiers

NCT06896591

COS-RGDS-2024-06-039-P-ELMALEH

Details and patient eligibility

About

This study aims to evaluate the effectiveness of a posterior hip capsule block performed in addition to a PENG (Pericapsular Nerve Group) block for patients undergoing hip arthroplasty. The primary objective is to assess whether this combined approach provides enhanced perioperative analgesia compared to the standard analgesic protocol or the PENG block alone. Secondary outcomes will focus on opioid consumption, functional recovery, and any potential complications. By targeting both the anterior and posterior innervation pathways around the hip joint, this combined technique could improve patient comfort, decrease opioid requirements, and potentially expedite rehabilitation after hip arthroplasty.

Enrollment: 35 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

All adults with total hip arthroplasty

Exclusion criteria

• Contraindication to regional anesthesia
• allergy
• refusal of the injection

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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35 participants in 1 patient group

DPPG compartment block

Experimental group

Description:

Deep posterior post gluteal compartment block with different volume of product 5,10 and 15 ml (local anesthetics such as naropeine 0.35%) to compare the efficiency of the block without sciatic nerve block effect

Treatment:

Procedure: Deep posterior post gluteal nerve block