About this trial
This randomized clinical trial (RCT) aims to compare clinical and radiographic outcomes of different partial wrist fusion techniques in participants with post-traumatic wrist arthritis. Participants with stage II or III scapholunate advanced collapse (SLAC) or scaphoid nonunion advanced collapse (SNAC) who meet the eligibility criteria will be randomly assigned to one of two parallel groups: Group A (partial wrist arthrodesis without triquetral excision i.e. four-corner arthrodesis), or Group B (partial wrist arthrodesis with triquetral excision i.e. three-corner or capitolunate arthrodesis with triquetral excision). The results of this study will provide evidence to guide surgeons in determining the ideal wrist fusion technique in the management of patients with post-traumatic wrist arthritis requiring surgery.
Eligibility criteria
Qualifiers
Participant has a stage II or III scapholunate advanced collapse (SLAC) or scaphoid nonunion advanced collapse (SNAC) wrist and is a surgical candidate for the included surgical interventions
Disqualifiers
Participant has been diagnosed with other forms of wrist arthritis other than SLAC or SNAC
Participant has significant arthritis of the ipsilateral hand/finger joint(s), major joint trauma, previous major wrist surgery, infection or neuromuscular pathology affecting the function of the ipsilateral upper extremity or ability to make a fist
Participant has a physical or mental health condition preventing completion of consent or questionnaires
Participant does not speak/read/understand English
Trial design
Treatments tested in this trial
- Four-Corner Arthrodesis
- Three-Corner or Capitolunate Arthrodesis with Triquetral Excision
Treatment groups
Sponsors and collaborators
University of Alberta
Lead sponsor
Arthritis Society Canada
Collaborator
Wrist Evaluation Canada (WECAN)
Collaborator