Investigating the Effect of Pericapsular Nerve Group (PENG) Block on Postoperative Pain After Peri-acetabular Osteotomy

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorMatias Vested

About this trial

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).

Eligibility criteria

Qualifiers

Patients ≥ 18 years old

Informed consent

Scheduled for periacetabular osteotomy under general anesthesia with intubation

American Society of Anesthesiologists (ASA) physical status classification I to III

Disqualifiers

Known allergy to ropivacaine

Daily use of opioids, gabapentin or tricyclic antidepressant (regardless of dose) within the last four weeks prior to surgery

Contraindications to Celocoxib, NSAIDs or paracetamol

Trial design

Treatments tested in this trial

  • Ropivacaine 5mg/ml 20ml
  • Saline 0.9%

Treatment groups

90 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Matias Vested

Lead sponsor

Rigshospitalet, Denmark

Sponsor institution