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

NCT ID: NCT06896591

Last Updated: 2025-03-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-01

Study Completion Date

2026-03-01

Brief Summary

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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.

Detailed Description

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Conditions

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Total Hip Arthroplasty

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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DPPG compartment block

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

Group Type EXPERIMENTAL

Deep posterior post gluteal nerve block

Intervention Type PROCEDURE

One injection with ultrasound guidance injection of 5, 10 or 15 mL of naropeine 0.35 % Procedure : injection below the piriformis muscle in front of the head of the femur.

Interventions

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Deep posterior post gluteal nerve block

One injection with ultrasound guidance injection of 5, 10 or 15 mL of naropeine 0.35 % Procedure : injection below the piriformis muscle in front of the head of the femur.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

All adults with total hip arthroplasty

\-

Exclusion Criteria

* Contraindication to regional anesthesia
* allergy
* refusal of the injection
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Quincy Anesthésie

NETWORK

Sponsor Role lead

Responsible Party

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Yoann ELMALEH

Medical Doctor, Anesthesiology and Pain Medicine, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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yoann ELMALEH, M.D

Role: PRINCIPAL_INVESTIGATOR

Hopital Privé Claude Galien

Central Contacts

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YOANN ELMALEH, M.D

Role: CONTACT

+33781330431

References

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Pun M, Ng T, Vermeylen K, Tran J. Innervation of the hip joint: implications for regional anaesthesia and image-guided interventional pain procedures. BJA Educ. 2024 Jun;24(6):191-202. doi: 10.1016/j.bjae.2024.02.005. Epub 2024 Apr 8. No abstract available.

Reference Type BACKGROUND
PMID: 38764441 (View on PubMed)

Other Identifiers

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

Identifier Type: -

Identifier Source: org_study_id

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