A Blinded Randomized Study Investigating the Effect of Pericapsular Nerve Group (PENG) Block on Postoperative Pain After Peri-acetabular Osteotomy
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:
• 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
• Can read and understand Danish
Locations
Other Locations
Denmark
Rigshospitalet
RECRUITING
Copenhagen
Contact Information
Primary
Matias Vested
matias.vested@regionh.dk
+4535455747
Time Frame
Start Date: 2024-08-19
Estimated Completion Date: 2026-03-01
Participants
Target number of participants: 90
Treatments
Experimental: Ropivacaine group
Ropivacaine 5 mg/ml 20ml
Placebo_comparator: Saline group
NaCl 0.9%
Related Therapeutic Areas
Sponsors
Leads: Matias Vested