Microdevice for Psoriasis and Atopic Dermatitis

This study is testing a small device, about the size of a grain of rice, for people with atopic dermatitis (eczema) or psoriasis. This microdevice holds tiny amounts of FDA-approved medications like Triamcinolone, 5-Fluorouracil, Calcipotriene, and Tapinarof. These medications will be released directly into your skin at very low levels. The goal is to see if the device is safe and can help predict how your skin will react to standard treatments. We'll also look at how these reactions relate to your genetic information and overall treatment results. The study aims to enroll 10 participants and is currently unclear on its recruitment status.

Study design
This interventional study plans to enroll 10 participants to test a microdevice directly on the skin.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for adverse events and device assessment for up to 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07352566

Utilization of a Microdevice for Psoriasis and Atopic Dermatitis

Not Yet Recruiting
PHASE4Ages 18+InterventionalDevice feasibility
University of California, San Francisco
~10 participants
Updated 2026-06-03 on ClinicalTrials.gov
What's tested:In situ cutaneous microdeviceTriamcinolone5-FluorouracilCalcipotrieneTapinarofCrisaborole

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of participants with adverse events
Measured over 1 year
+1 more outcome measured
Psoriasis
Atopic Dermatitis
1 sites across 1 states
California1
  • Raymond Cho, MD, PhD · PRINCIPAL_INVESTIGATOR · University of California, San Francisco

Opens a ready-to-send draft in your own email app — review before sending.

  • Number of participants with adverse events1 year

    The safety of microdevice placement and removal will be based on assessment of adverse events.

  • Proportion of retrieved devices with assessable tissue1 year

    The feasibility of microdevice analysis based on the ability to place and retrieve the device with sufficient tissue, of sufficient quality, for downstream histopathology/molecular analysis and interpretation of at least 80% of the device reservoirs.