Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
NCT06931418

Early Strengthening Rehabilitation Training for Post-operative Fracture Distal Radius

Led by The University of Hong Kong · Updated on 2025-04-25

50

Participants Needed

1

Research Sites

179 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary objective of this study is to demonstrate safety and efficacy of an early strengthening and passive mobilization rehabilitation program for post-operative distal radius fracture fixation surgery compared to current conventional rehabilitation.

CONDITIONS

Official Title

Early Strengthening Rehabilitation Training for Post-operative Fracture Distal Radius

Who Can Participate

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 50 years or older
  • Diagnosed with an isolated closed injury, displaced, distal radius fracture (AO/OTA Classification 23-A1-3, B1-2, C1-2) without articular comminution
  • Requires operative fixation
  • Able to give consent
Not Eligible

You will not qualify if you...

  • History of previous hand or wrist surgery
  • Neurological injury or pre-existing neurological conditions to the upper limb
  • Underlying osteoarthritis of the wrist
  • Unfit for surgical anesthesia
  • Subacute fractures with delayed presentation (>2 weeks since initial injury)
  • Unable to consent
  • Refuse surgical intervention
  • Unable to follow commands for rehabilitation
  • Fixation construct or injuries requiring immobilization after surgery, such as unfixed distal ulna head or shaft fractures that require splintage or distal radio-ulnar joint instability planned for immobilization

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Queen Mary Hospital, The University of Hong Kong

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

C

Christian Prof. Fang, MBBS(HK)

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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