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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorQuincy Anesthésie

About this trial

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.

Eligibility criteria

Qualifiers

None

Disqualifiers

Contraindication to regional anesthesia

allergy

refusal of the injection

Trial design

Treatments tested in this trial

  • Deep posterior post gluteal nerve block

Treatment groups

35 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators