CMC Arthroplasty for Thumb Arthritis
(SBSvsLRTI Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests two common surgeries for treating thumb arthritis, which causes pain and limits thumb joint movement. It compares trapezial excision (removal of a small wrist bone), with or without extra soft tissue work, to a newer method called suture button suspension (using a small button and thread to stabilize the thumb). The goal is to determine which surgery provides better long-term relief. Patients with thumb arthritis for at least six months, who haven't found relief from other treatments, might be suitable candidates. As an unphased trial, this study offers patients the chance to explore innovative surgical options that could enhance their quality of life.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. Please consult with the trial coordinators for more details.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research shows that both surgical treatments for thumb arthritis in this trial are generally safe. Studies have found trapezial excision to be a dependable option. Patients usually experience little to no pain and have minimal difficulty using their thumb after surgery. Nearly 94% of these surgeries last about 10 years without needing another procedure.
Similarly, the suture button suspension arthroplasty (SBS) demonstrates good safety results. Patients who undergo this surgery often report excellent long-term benefits, with significant improvements in thumb movement and reduced pain over time.
Both treatments have strong safety records, with most patients handling them well and experiencing few major problems.12345Why are researchers excited about this trial?
Researchers are excited about these treatments for thumb arthritis because they offer innovative methods compared to traditional options like fusion or trapeziectomy. The trapezial excision with soft tissue interposition and/or ligament reconstruction allows surgeons to use tendons like the FCR or APL to customize the procedure based on the patient's needs, potentially improving joint stability and function. Meanwhile, the suture button suspension arthroplasty (SBS) uses a suture button system to stabilize the joint, which could offer a less invasive alternative with quicker recovery times. These techniques may provide more flexibility and better outcomes for patients than the standard procedures currently in use.
What evidence suggests that this trial's treatments could be effective for thumb arthritis?
This trial will compare two treatments for thumb arthritis. Research has shown that trapezial excision, with or without additional procedures like soft tissue interposition or ligament reconstruction, leads to better outcomes. This method is known for its good long-term results and manageable side effects.
The trial also includes suture button suspension arthroplasty (SBS) as a treatment option. Research on SBS shows promising results, with patients often experiencing excellent long-term benefits. This method effectively improves thumb function and reduces pain. Both treatments in this trial have proven effective for managing thumb arthritis, offering patients reliable surgical choices.12367Are You a Good Fit for This Trial?
This trial is for individuals over 50 with isolated thumb arthritis who haven't improved with non-surgical treatments. Participants must be able to consent, follow the study plan, and attend clinical visits. Those with advanced arthritis stages, previous CMC surgeries, other hand conditions, inflammatory diseases or unable to maintain follow-up are excluded.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo either suture button suspension arthroplasty (SBS) or ligament reconstruction and tendon interposition (LRTI) for CMC arthritis
Follow-up
Participants are monitored for safety and effectiveness after treatment, with patient-reported outcomes collected at 6 weeks, 3, 6, and 12 months
What Are the Treatments Tested in This Trial?
Interventions
- CMC Arthroplasty
Find a Clinic Near You
Who Is Running the Clinical Trial?
Fraser Orthopaedic Research Society
Lead Sponsor