Wood casting takes on plastic splints in thumb surgery showdown
NCT ID NCT06876350
First seen Sep 25, 2026 · Last updated Sep 25, 2026
Summary
Researchers compare two types of splints, wood casting and standard thermoplastic, for people recovering from carpometacarpal arthroplasty, a surgery for thumb joint arthritis. Adults over 18 who are eligible for surgery join the study and wear one of the splints for six weeks. The team measures patient satisfaction and the amount of waste each splint creates.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- wood casting splint
- What this could lead to
- If wood casting works well, it could offer a more comfortable and less wasteful alternative to standard plastic splints after thumb joint surgery.
- What could go wrong
- This is a small study of 26 people, so its results may not apply broadly. Splint choice is unlikely to change the underlying arthritis, and individual healing varies.
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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About 26 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2024
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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: * Patients over the age of 18 years old. * Intact Medical Decision Making * Eligible for Surgical Intervention * Willing to comply with all aspects of the treatment and evaluation schedule over 6 weeks Exclusion Criteria: * Pregnant Women * Deemed Unsuitable by Principal Investigator
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Florida Orthopaedic Institute
RECRUITINGTampa, Florida, 33637, United States
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