Actively Recruiting
TRACE - Thumb Base Replacement Arthroplasty for Osteoarthritis.
Led by Karolinska Institutet · Updated on 2025-09-23
90
Participants Needed
1
Research Sites
700 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Osteoarthritis in the base of the thumb is one of the most common forms of hand arthritis. It usually appears in middle age, particularly in women, and can cause significant pain and loss of function. Early treatment often includes splints, painkillers, joint protection techniques, or steroid injections. If these measures are not enough, surgery is considered. The current standard operation in Sweden is trapeziectomy-removing the trapezium. This usually gives good pain relief at rest, but many patients continue to experience pain when loading the hand and reduced grip strength. Another surgical option is trapeziometacarpal limited excision (TLE), where only part of the bone is removed to keep the thumb slightly longer, which may improve strength. Both procedures are non-implant surgeries. A newer alternative is total joint arthroplasty (TJA), where the joint is replaced with a prosthesis. Early studies suggest that this may allow for quicker recovery and possibly better strength compared to trapeziectomy. However, it is more expensive and carries higher risks, such as implant loosening or dislocation. So far, research has not proven that it offers better long-term results. The TRACE study (A single arm trial of Thumb base Replacement Arthroplasty for osteoarthritis Compared to External controls) is designed to help answer this question. Instead of randomizing patients, this study will follow a group of people receiving thumb joint replacement and compare them to an existing group of patients who already took part in a randomized trial of trapeziectomy and TLE. This design allows the researchers to study results more quickly and with fewer resources, while still ensuring meaningful comparisons. The main research question of this study is whether joint replacement gives better pain relief when loading the thumb 10 years after surgery compared to traditional non-implant operations in patients with painful thumb base osteoarthritis. Secondary questions include whether joint replacement improves patient-reported outcomes, hand function, and strength, and whether it leads to more or fewer complications at 1, 3, and 5 years after surgery. 90 patients will be included in the replacement group, using a dual mobility prosthesis. Their outcomes will be compared with 90 patients from the earlier trial (45 trapeziectomy and 45 limited trapeziometacarpal joint resection - TLE). The study will track pain, daily hand function, strength, range of motion, and complications such as infection or the need for further surgery. Data will be collected regularly for up to 10 years.
CONDITIONS
Official Title
TRACE - Thumb Base Replacement Arthroplasty for Osteoarthritis.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Osteoarthritis in the thumb base with radiological Eaton class 1-3
- Clinical signs of thumb base osteoarthritis including pain at palpation of the CMC-1 joint and pain during provocation or grinding test
- Inclusion criteria match those of the control population
You will not qualify if you...
- Rheumatoid arthritis
- Ongoing infection in the hand or wrist
- History of gout or pseudogout in the hand
- Inability to cooperate with follow-up due to language difficulties, severe psychiatric disorder, cognitive impairment, or drug addiction
- Chronic pain syndrome or centralized pain
- Intra-articular corticosteroid injection in the affected joint within 3 months
- Eaton Littler class 4 symptomatic STT joint osteoarthritis
- Severe trapezium deformation preventing prosthetic cup placement
- Exclusion criteria match those of the control population
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Handkirurgiska kliniken Södersjukhuset
Stockholm, Sweden, 11883
Actively Recruiting
Research Team
M
Maria Wilcke, MD, Associate professor
CONTACT
J
Johanna Von Kieseritzky, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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