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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05250492
Acronym
API
Enrollment
60
Registered
2022-02-22
Start date
2022-03-02
Completion date
2023-05-15
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia, Hip Prosthesis, PENG Block

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.

Interventions

PROCEDUREProsthetic hip surgery

Total hip prosthesis performed by an anterior approach with intra-articular infiltration of an anesthetic product intraoperatively. OR \- Total hip prosthesis performed by an anterior approach with infiltration of the same anesthetic product by ultrasound-guided PENG block intraoperatively.

Sponsors

GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead SponsorOTHER
European Clinical Trial Experts Network
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative morphine consumption in the postoperative care unit1 hourPostoperative morphine consumption (in mg) in the postoperative care unit

Secondary

MeasureTime frameDescription
Postoperative morphine équivalent consumption at postoperative day 11 daypostoperative morphine équivalent consumption (in mg) at postoperative day 1

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026