Eczema Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 12 to 89 years old.
- People who have been diagnosed with atopic dermatitis (eczema).
- People who have had at least one eczema flare-up in the past 2 months.
- People who are willing and able to use a home monitoring device called Nevisense Go, fill in a daily symptom diary on an electronic device, and attend study appointments.
- People who are currently on a systemic (whole-body) treatment for eczema, provided that treatment has stayed the same for at least 3 months and there are no plans to change it during the study.
Who may not be able to join:
- People who are unwilling or unable to avoid applying creams, lotions, ointments, or soap to the skin areas being measured for 6 hours before each measurement.
- People who do not have suitable skin areas available for the study's measurements (confirm with trial site).
- People who have another skin condition that could affect how the study assessments are interpreted.
- People who are pregnant.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 602-499-0301
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Relationship between skin measurements and subsequent atopic dermatitis flares; Develop and validate an algorithm using Nevisense Go EIS
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.