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 个研究点目标入组 120 人开始时间: 2021年2月18日最近更新: 2021年2月22日

适应症

试验速览

暂无简介。

•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

•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

发起方

Trauma and Orthopaedic Research Unit Canberra Hospital