Skip to main content
Clinical Trials/NCT05250492
NCT05250492
Completed
Not Applicable

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

Ramsay Générale de Santé1 site in 1 country60 target enrollmentMarch 2, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Prosthesis
Sponsor
Ramsay Générale de Santé
Enrollment
60
Locations
1
Primary Endpoint
Postoperative morphine consumption in the postoperative care unit
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 2, 2022
End Date
May 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Postoperative morphine consumption in the postoperative care unit

Time Frame: 1 hour

Postoperative morphine consumption (in mg) in the postoperative care unit

Secondary Outcomes

  • Postoperative morphine équivalent consumption at postoperative day 1(1 day)

Study Sites (1)

Loading locations...

Similar Trials