Pericapsular Nerve Block Versus Intrathecal Morphine for Analgesia After Primary Hip Arthroplasty
Recruiting
N/A
Interventional Study
Analgesia
Hip Arthropathy
Post Operative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 80 (estimated)
- Sponsor
- Centre Hospitalier Universitaire Vaudois · Other
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About This Trial
The aim of this clinical trial is to compare the analgesic effect of pericapsular nerve block (PENG) with intrathecal morphine in patients scheduled for total hip replacement surgery. The main question to be answered is whether the PENG block is equivalent to intrathecal morphine in reducing postoperative pain.
Participants will be randomised into two groups. Patients assigned to the PENG group w…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Male and female patients
* ASA (American Society of Anaesthesiologists) I-III
* 18 years of age or older
* Patients scheduled for elective primary hip arthroplasty
* Able to give written conformed consent autonomously
Exclusion Criteria:
* Refusal or inability to give consen…
Contacts