Gout sufferers could soon track uric acid with a simple skin patch
NCT ID NCT06187519
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a new skin patch system called UR+AIMS that measures uric acid levels in people with gout. Six participants wore the patch for a week and during a standard meal to see if it was comfortable and gave accurate readings. The goal is to help patients better understand how their diet and medications affect their uric acid levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Uric Acid and Metabolite Monitor System (UR+AIMS) skin patch
- What this could lead to
- If it works, this could lead to a simple skin patch that helps people with gout track their uric acid levels in real time, making it easier to manage their condition through diet and medication.
- What could go wrong
- This is a very small, early-stage lab validation study with only 6 participants, so results may not apply to everyone. The patch might be uncomfortable or inaccurate, and it's not yet proven to improve health outcomes.
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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6 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Sep 2025
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age \> 18 with diagnosis of gout (screening positive ACR/EULAR Gout Classification Criteria - see screening survey) and eGFR \> 60 (within the last 12-months). 2. For the 10 patients with gout off urate-lowering therapy (ULT) \[no Allopurinol, febuxostat, or probenecid prescription within the last 6-months\] and serum urate (SU) \> 7 mg/dL (within the last 12-months). 3. For the 5 patients with gout on urate-lowering therapy (ULT) \[no dose change within the last 30 days\]. Exclusion Criteria: 1. Contraindications to miosis, which include acute iritis, narrow-angle glaucoma 2. Known Hypersensitivity to pilocarpine hydrochloride 3. Pupillary block glaucoma (ophthalmic solution) 4. Subjects reporting any allergy to glue or latex or any allergy to food that will be provided in the study (sardines in extra virgin olive oil and Sprite).
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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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UCLA
Los Angeles, California, 90095, United States
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Other studies related to the condition(s) this trial covers.
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