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New wearable device aims to soothe knee arthritis without drugs
NCT ID NCT06475677
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a portable device called the OrthoCor Advanced System in 23 people with knee osteoarthritis. The device delivers pulsed electromagnetic fields and heat to the knee, and users track their progress with a smartphone app. Researchers measured pain, range of motion, and function after 4 weeks of twice-daily use to see if symptoms improved.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- OrthoCor Advanced System (PEMF and heat therapy device)
- What this could lead to
- If it works, this could offer a non-invasive, drug-free option for managing knee osteoarthritis pain at home.
- What could go wrong
- This was a small, early study with only 23 participants and no comparison group, so results may not apply widely. The device is not a cure and only aims to ease symptoms temporarily.
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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23 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Oct 2025
- 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
-
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 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: 1. Presenting to the study site with knee pain for at least 3 months, with articular cartilage loss confirmed by imaging study 2. An initial pain VAS score \>4 3. At least 2 hours of daily standing and/or walking activity 4. Prescribed use of the OrthoCor Advanced System 5. Daily access to a smartphone or tablet compatible with the OrthoCor Medical application 6. Able to download and install app to smart phone 7. Willing and able to provide written consent 8. ≥18 years of age Exclusion Criteria: 1. Previous diagnosis of rheumatoid arthritis or gout 2. Cortisone injection, knee surgery, or viscosupplementation in the previous 6 months 3. Prior knee replacement 4. Have a cardiac pacemaker, cardioverter defibrillator, neurostimulator, infusion pump or any active medical implant 5. Have an implanted metallic lead or any type of wire coil implant, or any implanted system that may contain a lead 6. Known or expected pregnancy 7. Have an open wound at the area of application 8. Are not able to sense or not fully aware of the sensation of heat 9. Have poor circulation or heart disease 10. Have uncontrolled diabetes 11. Under the age of 18 or individuals with open bone growth plates 12. Unwilling or unable to provide written consent 13. Unwilling or unable to use the OrthoCor Advanced System 14. Unwilling or unable to complete the pain assessment survey 15. Enrolled in a study to evaluate an investigational drug 16. Prisoner or under incarceration
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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
-
Andrews Research & Education Foundation
Gulf Breeze, Florida, 32561, United States
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