New brace gently massages wrist while you sleep to ease carpal tunnel pain
NCT ID NCT06208709
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a new brace that applies small, repeated forces to the wrist during sleep, aiming to relieve carpal tunnel syndrome symptoms. Researchers will compare it to a standard brace in 116 adults. The main goal is to see if the device reduces pain and improves hand function after 8 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A brace with a built-in balloon that applies gentle, repeated pressure to the wrist during sleep.
- What this could lead to
- If it works, this could offer a simple, non-surgical way to reduce pain and improve hand function for people with carpal tunnel syndrome.
- What could go wrong
- This is a small, early pilot study. The device may not provide meaningful relief, and results may not apply to everyone with carpal tunnel syndrome.
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 116 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2024
- Expected to finish
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Jul 2026
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 * 18 and older * Diagnosed with right-handed or bilateral CTS. Participants will be treated only in the right hand. Exclusion Criteria * History of musculoskeletal or neurological conditions that may confound Carpal Tunnel Syndrome symptoms, including but not limited to: 1. Diagnosed or suspected arthritis in the test wrist, hand, or finger joints 2. Prior neck trauma, whiplash injury, or any condition suggestive of cervical radiculopathy 3. Current or prior treatment from a healthcare provider such as neurologist, physical therapist, physiatrist, rheumatologist, neurosurgeon, orthopedic surgeon or chiropractor for cervical radiculopathy or other musculoskeletal problem involving the neck, shoulder, and or upper extremity * History of traumatic or chronic symptomatic neuromusculoskeletal disorders involving the upper extremity to be tested. * The following diseases: uncontrolled diabetes, thyroid disease, rheumatoid arthritis, gout, lupus, renal failure, hemodialysis, sarcoidosis, amyloidosis, additional systemic diseases that may have an effect on the peripheral median nerve. * Positive diagnosis of cervical disorders affecting the same side of the body as the test hand such as radiculopathy, spondylosis, tumor, and multiple sclerosis * Symptomatic joint diseases in the test hand (e.g., Osteoarthritis) * Osteoporosis in the test hand * History of carpal tunnel release in the test hand * History of corticosteroid injection treatments for CTS in the test hand within the 3 months preceding study initiation * Women who are currently pregnant * Patients who have carpal tunnel release surgery scheduled for the next 12 weeks in their test hand. * Patients who have taken pain medication, including over-the-counter products, within 2 weeks prior to initiation of the study. * Will not participate in other CTS treatment or therapies during this study
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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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University of Arizona
RECRUITINGTucson, Arizona, 85724, United States
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Other studies related to the condition(s) this trial covers.
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