Clinical Trial

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

Study acronym: ANATH
Not Yet Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated March 26, 2025 (before its estimated February 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
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.
Trial Details
NCT Number NCT06896591
Lead Sponsor Quincy Anesthésie
Conditions Total Hip Arthroplasty
Enrollment 35 participants
Start Date 2025-06-01
Primary Completion 2026-02-01 (estimated)
Study Completion 2026-03-01 (estimated)
Updated on ClinicalTrials.gov 2025-03-26