This study aims to determine the effectiveness and safety of two standard of care perioperative procedures for controlling pain following ankle and hindfoot osteotomy or fusion or ankle fracture repair.
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Visual Analog Score
Timeframe: Postoperative hour 3
Evidence of motor block
Timeframe: Postoperative hour 3
Visual Analog Score
Timeframe: Postoperative hour 6
Visual Analog Score
Timeframe: Postoperative hour 12
Visual Analog Score
Timeframe: Postoperative hour 24
Visual Analog Score
Timeframe: Postoperative hour 36
Visual Analog Score
Timeframe: Postoperative hour 48
Visual Analog Score
Timeframe: Postoperative hour 72
Visual Analog Score
Timeframe: Postoperative week 2
Visual Analog Score
Timeframe: Postoperative week 4-6
Visual Analog Score
Timeframe: Postoperative week 12