Evaluation of Analgesia by PENG Block Versus Intra-Articular Infiltration in Prosthetic Hip Surgery (API)

Not Applicable

Completed

• Conditions: Analgesia; PENG Block; Hip Prosthesis
• Interventions: Procedure: Prosthetic hip surgery

• Registration Number: NCT05250492
• Lead Sponsor: Ramsay Générale de Santé

Brief Summary

The main objective of this study is to compare the effectiveness of the ultrasound-guided PENG block technique compared to intra-articular infiltration on postoperative morphine consumption during hip prosthetic surgery via the anterior minimally invasive approach under general anesthesia.

Detailed Description

Not available

Study Timeline

• Status Verified: 2022-02
• Study First Submitted: 2022-02-10
• Study First Submitted QC: 2022-02-10
• Study First Posted: 2022-02-22
• Study Start: 2022-03-02
• Primary Completion: 2022-09-09
• Study Completion: 2023-05-15
• Last Update Submitted: 2024-12-03
• Last Update Posted: 2024-12-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Patient, male or female, over 18 years old.
• Patient scheduled for anterior hip prosthesis.
• Affiliated patient or beneficiary of a social security scheme.
• Patient having been informed and having signed a free and informed consent.

Exclusion Criteria

• Patient with a contraindication to local anesthesia.
• Patient with a high level of dependence, defined by level 1 or 2 of the Iso-Ressources Group (GIR).
• Patient participating in another clinical study.
• Protected patient: adult under guardianship, curatorship or other legal protection, deprived of freedom by judicial or administrative decision.
• Pregnant, breastfeeding or parturient woman.
• Patient hospitalized without consent.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Patients with intra-articular infiltration	Prosthetic hip surgery	-
Patients with PENG block	Prosthetic hip surgery	-

Primary Outcome Measures

Name	Time	Method
Postoperative morphine consumption in the postoperative care unit	1 hour	Postoperative morphine consumption (in mg) in the postoperative care unit

Secondary Outcome Measures

Name	Time	Method
Postoperative morphine équivalent consumption at postoperative day 1	1 day	postoperative morphine équivalent consumption (in mg) at postoperative day 1

Trial Locations

Locations (1)

Jean-François Oudet; 🇫🇷 Lanester, France