ACTRN12621000169842
Not yet recruiting
未知
A randomised control trial of post-operative complications and patient reported outcomes following total wrist arthrodesis in isolated wrist arthritis with spanning plate and carpometacarpal joint arthrodesis compared to non-spanning plate without carpometacarpal arthrodesis
Trauma and Orthopaedic Research Unit Canberra Hospital0 sites120 target enrollmentFebruary 18, 2021
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- wrist post traumatic arthritis
- Sponsor
- Trauma and Orthopaedic Research Unit Canberra Hospital
- Enrollment
- 120
- Status
- Not yet recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •This study will include English speaking, non\-institutionalized individuals aged \> 18 years deemed suitable for total wrist arthrodesis by their surgeon, with non\-inflammatory indications for surgery including:
- •SNAC (Scaphoid non\-union advanced collapse)
- •SLAC (Scapholunate ligament advanced collapse)
- •Keinbock’s disease/Lunate avascular necrosis
- •Preiser’s disease/Scaphoid avascular necrosis
- •Wrist osteoarthritis
- •Post traumatic arthritis
- •Failed partial fusion
Exclusion Criteria
- •Patients will be excluded from this study if:
- •Lack ability to consent for participation (cognitive capacity or English proficiency)
- •Lack ability to report patient outcomes measures (cognitive capacity or English proficiency)
- •Have an inflammatory arthropathy (i.e., Rheumatoid arthritis)
- •Have pre\-existing upper ipsilateral or contralateral limb pain or dysfunction
- •Brain, nerve or muscle dysfunction (CVA, plexus injury, peripheral nerve injury, spasm or contracture)
- •Tumour of the wrist (giant cell or other)
- •Wrist arthroplasty that will be revised to arthrodesis
- •Planned to undergo or have undergone bilateral wrist arthrodesis
Outcomes
Primary Outcomes
Not specified
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