Robotic help for bone break surgeries in orthopaedic trauma
Official title: Outcomes for Robotics in Orthopaedic Trauma
Run by Prince of Wales Hospital, Shatin, Hong Kong · NCT07732803 · Data updated 2026-11-12
This trial tests whether using a robotic system to aid reduction and fixation in orthopaedic trauma leads to better accuracy and recovery compared to standard methods.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Prince of Wales Hospital, Shatin, Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | June 15, 2026 |
| Main results expected | February 28, 2030 |
| Study ends | March 1, 2031 |
| Registry record updated | July 29, 2026 |
| Trial ID | NCT07732803 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with orthopaedic trauma and a fracture who are candidates for surgical intervention and willing to participate.
✕Probably not a fit
Patients for whom robotic assistance does not improve outcomes or those not undergoing surgery may not benefit.
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 robotic-assisted reduction and fixation in orthopaedic trauma surgeries. It compares robotic assistance with conventional approaches to see if it improves fracture reduction, surgical outcomes, and reduces complications. The trial focuses on minimally invasive techniques using the R-Universal Intelligent Robotic Surgical System. Participants are adults with orthopaedic trauma who require surgery, recruited at The Chinese University of Hong Kong with Prince of Wales Hospital as lead sponsor.
Why it matters
Potential benefit: If successful, robotic assistance could improve fracture reduction accuracy and shorten recovery time while lowering post-operative complications.
How similar studies have gone: Previous studies in robotics-assisted orthopedic procedures have shown mixed results, making this trial important to establish efficacy in trauma cases.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Males or females aged 18 years or older * With orthopaedic trauma and fracture * Willing to participate in the study Exclusion Criteria: * Cognitive problems e.g., severe dementia (unable to agree for consent) * Unable to agree for consent * Surgeons decide that surgery is not indicated for the patients
Where it's running
-
The Chinese University of Hong Kong
Hong Kong, China Recruiting
Study contacts
- Study coordinator: Ronald Man Yeung Wong
- Email: ronald.wong@cuhk.edu.hk
- Phone: 852 35051654
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.