Sound wave therapy shows promise for arthritis inflammation
NCT ID NCT06555562
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
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16 people
The number who actually took part.
- Started
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Oct 2025
- Finished
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Jan 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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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 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.
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
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Tekton Research
Austin, Texas, 78745, United States
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UT Health
Houston, Texas, 77030, United States
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Other studies related to the condition(s) this trial covers.
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