Actively Recruiting
Investigating the Effect of Pericapsular Nerve Group (PENG) Block on Postoperative Pain After Peri-acetabular Osteotomy
Led by Matias Vested · Updated on 2025-08-26
90
Participants Needed
1
Research Sites
79 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to determine the effect of PENG blockade on postoperative pain after either ropivacaine 5 mg/mL or saline (placebo) in patients undergoing PAO. The hypothesis of this study is that PENG block with ropivacaine reduces postoperative pain compared to placebo (saline).
CONDITIONS
Official Title
Investigating the Effect of Pericapsular Nerve Group (PENG) Block on Postoperative Pain After Peri-acetabular Osteotomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older
- Provided informed consent
- Scheduled for peri-acetabular osteotomy under general anesthesia with intubation
- American Society of Anesthesiologists (ASA) physical status classification I to III
- Can read and understand Danish
You will not qualify if you...
- Known allergy to ropivacaine
- Daily use of opioids, gabapentin, or tricyclic antidepressants within the last four weeks before surgery
- Contraindications to Celocoxib, NSAIDs, or paracetamol
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Rigshospitalet
Copenhagen, Denmark, 2100
Actively Recruiting
Research Team
M
Matias Vested
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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