Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT04580225

Randomized Comparison of PARtial Wrist Fusion With or Without Triquetral Excision (PARTE)

Led by University of Alberta · Updated on 2025-11-18

170

Participants Needed

6

Research Sites

325 weeks

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

A

Arthritis Society Canada

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Randomized Comparison of PARtial Wrist Fusion With or Without Triquetral Excision (PARTE)

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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
  • Participant has no fixed address or means of contact
  • Participant is unwilling to complete necessary follow-ups
  • Surgeon concludes that eligible salvage techniques are not appropriate at the time of surgery (based on injury characteristics or concomitant wrist pathology)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 6 locations

1

Peter Lougheed Centre

Calgary, Alberta, Canada

Actively Recruiting

2

South Health Campus

Calgary, Alberta, Canada

Actively Recruiting

3

Western Hand & Upper Limb Facility, Sturgeon Community Hospital

St. Albert, Alberta, Canada

Actively Recruiting

4

Lawson Health Research Institute

London, Ontario, Canada

Actively Recruiting

5

The Ottawa Hospital - Civic Campus

Ottawa, Ontario, Canada

Actively Recruiting

6

University of Saskatchewan

Saskatoon, Saskatchewan, Canada

Actively Recruiting

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Research Team

D

Dr. Armin Badre, MD, MSc, FRCSC

CONTACT

C

Collaborative Orthopaedic Research (CORe)

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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