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Study Comparing SBS and LRTI for Treatment of CMC Arthritis

Arthritis

A multi-center, randomized control trial comparing the two standard of care surgical treatments for CMC arthritis ; trapezial excision with or without soft tissue interposition and /or ligament reconstruction (LRTI) versus the suture button suspension arthroplasty (SBS). Patient reported outcomes will be collected at 6 and 6 weeks, 3, 6, and 12 months.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    50 and up

Participation Criteria

Inclusion Criteria:

* Age fifty years or older
* Isolated carpometacarpal (trapeziometacarpal) osteoarthritis
* Failure to respond to non-operative management
* Willing and able to consent on their own behalf and follow the protocol and clinical visits as described
* Able to read and understand English or have interpreter available

Exclusion Criteria:

* Previous surgery for CMC arthritis
* Duration of symptoms for less than 6 months
* Greater than or equal to 30 degrees of ipsilateral metacarpophalangeal (MCP) hyperextension
* Scaphotrapeziotrapezoidal (stage 4 CMC) arthritis
* Other significant ipsilateral wrist or hand pathology
* A history of inflammatory arthropathy
* A requirement for concomitant surgery for another condition
* Any previous hand or wrist fracture
* Likely problems, in the judgement of the investigators, with maintaining follow-up (i.e. patients with no fixed address, not mentally competent to give consent, intellectually challenged patients without adequate support, etc.)

Study Location

Fraser Orthopaedic Research Society
Fraser Orthopaedic Research Society
New Westminster, British Columbia
Canada

Contact Study Team

Primary Contact

Bertrand Perey, MD

604-553-3247
Backup Contact

Kyrsten Butterfield, BSc

[email protected]
604-553-3247
South Campus Research Unit for Bone and Soft Tissue
South Campus Research Unit for Bone and Soft Tissue
Calgary, Alberta
Canada

Contact Study Team

Backup Contact

Adina Tarcea

[email protected]
403-956-3687
Primary Contact

Neil White

403-956-3687
Study Sponsored By
Fraser Orthopaedic Research Society
Participants Required
More Information
Study ID: NCT05111405