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Recruiting Not applicable

Outcomes for Robotics in Orthopaedic Trauma

NCT07732803 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-06-15
Last updated
2026-07-29

Condition(s) studied

Orthopaedic Trauma

Investigational drug(s) / intervention(s)

Robotic Assistance: The robotic system (R-Universal® Intelligent Robotic Surgical Systems, Beijing Rossum Robot Technology Co., Ltd.)

Robotic Assistance: The robotic system (R-Universal® Intelligent Robotic Surgical Systems, Beijing Rossum Robot Technology Co., Ltd.): The robotic system (R-Universal® Intelligent Robotic Surgical Systems, Beijing Rossum Robot Technology Co., Ltd.) will be moved to the site of injury and held to the pins placed onto bone as the preoperative plan. The reduction process will be completed under the supervision of 3D real-time navigation. The fracture is then fixated. The robotic arm will perform precise movements during surgery for reduction to try to reduce the chance of malalignment. Moreover, these robots can allow minimally invasive surgeries.

Study summary

Our project aims to integrate whether robotic assistance of reduction and fixation in orthopaedic trauma surgery can enhance accuracy and surgical outcomes. The current study aims to shorten the recovery time and reduce post-operative complications by minimally invasive surgery with robotics.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
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

Primary outcome measure(s)

  • Operation Time — Baseline
    Operation time will be documented from the Clinical Management System (CMS).
  • Blood Loss — Baseline
    Blood loss will be documented from the Clinical Management System (CMS).
  • Length of Hospital Stay — Baseline
    Length of hospital stay will be documented from the Clinical Management System (CMS).
  • Plain Radiographs — From baseline to 52-weeks post-operation
    Plain radiographs will be taken at the corresponding sites of injuries post operation. The reduction quality will be assessed based on Matta criteria
  • Computed Tomography (CT) — From baseline to 12-weeks post-operation
    CT scan will be taken at the corresponding sites of injuries pre- and post operation.

Trial sites (1)

FacilityCityRegionStatus
The Chinese University of Hong Kong Hong Kong China Recruiting

More Prince of Wales Hospital, Shatin, Hong Kong trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07732803 on ClinicalTrials.gov ↗ ← All trials in China