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

R

Ramsay Générale de Santé

Status

Completed

Conditions

Hip Prosthesis
Analgesia
PENG Block

Treatments

Procedure: Prosthetic hip surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT05250492
2021-A00539-32

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Patients with PENG block
Experimental group
Treatment:
Procedure: Prosthetic hip surgery
Patients with intra-articular infiltration
Active Comparator group
Treatment:
Procedure: Prosthetic hip surgery

Trial contacts and locations

1

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Central trial contact

Marie-Hélène Barba; Jean-François Oudet

Data sourced from clinicaltrials.gov

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