Effect of PENG Block on Pain After Hip Surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the impact of the pericapsular nerve group (PENG) block on postoperative pain management in patients undergoing peri-acetabular osteotomy (PAO). Participants will receive either ropivacaine or saline as a placebo to assess the effectiveness of the PENG block in reducing pain after surgery. The study aims to provide insights into the analgesic benefits of this novel regional anesthesia technique, which targets specific nerves innervating the hip joint. By comparing outcomes between the two groups, the research seeks to enhance postoperative pain management strategies for hip dysplasia surgeries.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Patients ≥ 18 years old
2. Informed consent
3. Scheduled for periacetabular osteotomy under general anesthesia with intubation
4. American Society of Anesthesiologists (ASA) physical status classification I to III
5. Can read and understand Danish

Exclusion Criteria:

1. Known allergy to ropivacaine
2. Daily use of opioids, gabapentin or tricyclic antidepressant (regardless of dose) within the last four weeks prior to surgery
3. Contraindications to Celocoxib, NSAIDs or paracetamol

Where it's running

• Rigshospitalet
  Copenhagen, Denmark Recruiting

Study contacts

• Study coordinator: Matias Vested
• Email: matias.vested@regionh.dk
• Phone: +4535455747

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.