New pain block could cut morphine use after hip surgery
NCT ID NCT05250492
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This trial compares two ways to manage pain during hip replacement surgery: an ultrasound-guided nerve block (PENG block) versus injecting anesthetic directly into the joint. The study includes 60 adults scheduled for anterior hip replacement under general anesthesia. The main goal is to see which method reduces the need for morphine right after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ultrasound-guided PENG block (pericapsular nerve group block) with anesthetic
- What this could lead to
- If the PENG block proves better, it could become the standard method for controlling pain after hip replacement, reducing reliance on morphine.
- What could go wrong
- This is a small, early-stage comparison, so results may not apply to all patients or surgical approaches. The PENG block might not offer significant advantages over the simpler infiltration method.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
60 people
The number who actually took part.
- Started
-
Mar 2022
- Finished
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May 2023
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Jean-François Oudet
Lanester, 56600, France
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