New thumb implant aims to ease arthritis pain
NCT ID NCT06467760
First seen Jun 26, 2026 · Last updated Jul 23, 2026 · Updated 2 times
Summary
This study is testing a new thumb implant called the InDx CMC Implant for people with thumb arthritis. The implant replaces part of the thumb joint to improve hand function and reduce pain. Researchers will track safety and how well the implant works in 73 adults over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- InDx CMC Implant (a thumb joint replacement device)
- What this could lead to
- If this works, it could offer a new surgical option for thumb arthritis that may improve hand function and reduce pain.
- What could go wrong
- This is a small, early-stage study with no comparison group. The implant could fail or require revision surgery. Results may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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14 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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May 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * The patient is at least 18 years of age; * The patient has a confirmed Grade I-III osteoarthritis of the CMC joint on clinical examination and X-ray; * The patient is eligible for surgical treatment of CMC I arthrosis in the opinion of the investigator. * The patient agrees to abstain from enrolment in any other clinical trials that will conflict or interfere with the interpretation of the results of this study, in the opinion of the Investigator, for the duration of the study; * The patient is able to understand the aims and objectives of the trial and is willing to consent; * The patient is willing and able to return for all study-related follow-up procedures; * If the patient is female, is either using contraception or is postmenopausal, or male partner is using contraception Exclusion Criteria: * The patient is suffering from Rheumatoid arthritis in the index hand; * The patient is suffering from Grade IV osteoarthritis of the CMC joint; * The patient is suffering post-traumatic arthritis of the CMC joint in the index hand; * The patient is a pregnant/lactating female (tested as per institutional requirements); * Active or latent infection, or sepsis; * Insufficient quantity or quality of bone and/or soft tissue in the index hand; * Metal or polymer material sensitivity; * Muscular imbalance, peripheral vascular disease that prohibits adequate healing, or a poor soft-tissue envelope in the surgical field, absence of musculoligamentous supporting structures, or peripheral neuropathy; * Patient with previous thumb surgery in the index hand * In the opinion of the investigator, any medical condition that makes the subject unsuitable for inclusion in the study, including, but not limited to * Patients with a diagnosis of concomitant injury that may interfere with healing * Patients with clinically significant renal, hepatic, cardiac, endocrine, hematologic, autoimmune, or any systemic disease or systemic infection that may make interpretation of the results difficult * Patients who have undergone systemic administration within 30 days prior to implantation of any type of corticosteroid, antineoplastic, immunostimulating, or immunosuppressive agents * Comorbidity that reduces life expectancy to less than 36 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Az Sint-Jan Brugge AV
Bruges, 8000, Belgium
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Bergman Clinics
Amsterdam, 1101GB, Netherlands