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New thumb implant aims to ease arthritis pain

NCT ID NCT06467760

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

14 people

The number who actually took part.

Started

Mar 2025

Finished

May 2026

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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

  • Az Sint-Jan Brugge AV

    Bruges, 8000, Belgium

  • Bergman Clinics

    Amsterdam, 1101GB, Netherlands