The objective of this study is to demonstrate the safety and efficacy of an intra-articular analgesics cocktail injection for post-operative patella fracture fixation patients, by comparing post-operative pain relief and functional recovery among study subjects who received the injection and those who did not receive the injection. Secondary objective is to demonstrate the health economic effects of intra-articular analgesics cocktail injection by reducing length of hospital stay and reducing bed-stay related complications.
Age range
18 Years
Sex
ALL
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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.
Pain as measured by Numerical Patient Reported Scale (NRPS)
Timeframe: Pre-op, Post-op Day 1 to 3
Maximum Active Knee Flexion
Timeframe: At post-op Day 1 to 3
Oral analgesics consumed
Timeframe: Post-operative 2 weeks period
Tegner Lysholm Knee Score
Timeframe: Post-op Day 14
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Timeframe: Post-op Day 14
9-item Quality of Recovery Score (QoR-9 Score)
Timeframe: Post-op Day 1 to 3