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Sound wave therapy shows promise for arthritis inflammation

NCT ID NCT06555562

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 This study
The trial has finished. Results may not be published yet.
Stopped early
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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested whether a non-invasive ultrasound device can reduce inflammation in people with inflammatory arthritis (psoriatic arthritis, rheumatoid arthritis, or ankylosing spondylitis). Sixteen participants received four sessions of focused ultrasound or a sham (placebo) treatment. The main goal was to see if ultrasound could lower levels of inflammatory markers in the blood. This is an early-stage study focused on understanding the body's response, not on treating symptoms.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
focused ultrasound stimulation
What this could lead to
If it works, this could point toward a non-drug way to control inflammation in arthritis.
What could go wrong
This is a very small, early study in healthy volunteers and people with arthritis. It only measures short-term changes in blood markers, not actual symptom improvement. The results may not lead to a treatment.

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

16 people

The number who actually took part.

Started

Oct 2025

Finished

Jan 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

22 to 75 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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.

Healthy Volunteer Population Inclusion Criteria: * 22-75 years of age * Weigh at least 40 kg Exclusion Criteria: * Any physical disabilities, conditions, or diseases that limit the capacity to participate in study procedures or increase the risk of harm as determined by the study PI * Unable to provide informed consent * Active bacterial or viral infection * Class II obesity with a BMI of 35 or higher * Pregnant women or those trying to become pregnant * Active use of tobacco/nicotine products * History of substance use disorder or active regular use of substances (nicotine, marijuana, cocaine, psychedelics, stimulants, etc.) * Splenomegaly, asplenia, or splenectomy Inflammatory Arthritis Population Inclusion Criteria: * 22-75 years of age * Weigh at least 40 kg * Diagnosis of Rheumatoid Arthritis, Psoriatic Arthritis, or Axial Spondyloarthritis of at least 6 months duration as defined by ACR guidelines * Able to continue the same stable dose of immunomodulatory medication(s) while participating in the study Exclusion Criteria: * Unable to provide informed consent * Took a JAK inhibitor within the last 4 weeks, or likely to start one while participating in this study * Started a conventional synthetic DMARD (csDMARD) within the last 8 weeks or had a change in prescription within the last 4 week * Started a Tumor Necrosis Factor (TNF) inhibitor within the last 5 months or had a change in prescription within the last 3 months * Started any other biologic or targeted synthetic DMARD within the last 3 months, or likely to start one while participating in the study * Started a corticosteroid, had a change in prescription, or on a stable dose = or \> 10 mg of prednisone daily within the last 4 weeks * Regular use of epinephrine like medications (cold, cough, congestion, or sinus medications, bronchodilators, appetite suppressants) * Active use of tobacco/nicotine products * History of substance use disorder or likely use of substances during the study period (marijuana, opioids/heroin, cocaine, psychedelics, methamphetamine, etc.) * Active bacterial or viral infection * Receiving chemotherapy or immunotherapy to treat malignancy * Significant immunodeficiency due to underlying illness * Class II obesity with a BMI of 35 or higher * Pregnant women or those trying to become pregnant * Wound, rash, infection, or traumatic injury over the target area * Vagal nerve injury or vagotomy * Surgery or major traumatic injury in the past 90 days * Chronically-implanted medical devices (i.e. pacemaker, AICD, vagus nerve stimulator, spinal cord stimulator) * Clinically significant cardiovascular disease * CKD Stage 3 or higher * Uncontrolled fibromyalgia or other diffuse pain syndromes

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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

  • Tekton Research

    Austin, Texas, 78745, United States

  • UT Health

    Houston, Texas, 77030, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.