Clinical trial Recruiting at 1 site Observational Ages 1 Year to 26

Registry for patients with pediatric atopic dermatitis receiving systemic treatments

Official title: Registry for Systemic Eczema Treatments

Run by Johns Hopkins University · NCT06136767 · Data updated 2026-11-12

This study is creating a registry for kids with severe eczema who are using or planning to use systemic treatments to help researchers learn more about how well these treatments work and keep everyone updated on new options.

More Atopic Dermatitis trials

Quick facts

Study typeObservational
Ages1 Year to 26 Years
SexAll
Enrollment400 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations1 site (Baltimore, Maryland)
StatusRecruiting
StartedJanuary 17, 2024
Main results expectedAugust 31, 2030
Study endsDecember 31, 2030
Registry record updatedApril 7, 2026
Trial IDNCT06136767 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this registry are individuals under 26 years old with a physician diagnosis of atopic dermatitis who have received care at Johns Hopkins since January 1, 2017.

Probably not a fit

Patients over 26 years old or those who have not received care at Johns Hopkins since January 1, 2017, may not benefit from this registry.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Registry for Systemic Eczema Therapies (RESET) is a comprehensive database and biospecimen repository aimed at patients with pediatric-onset atopic dermatitis (AD) who are using or planning to use systemic treatments. This registry will facilitate efficient recruitment for research studies and enable timely notifications about new FDA-approved therapies for AD. It will collect data to compare treatment effectiveness and monitor safety profiles of both traditional and novel systemic agents. Additionally, it aims to identify patients with moderate-to-severe AD who may benefit from emerging therapies.

Why it matters

Potential benefit: If successful, this registry could enhance treatment options and outcomes for patients with atopic dermatitis by facilitating research and improving access to new therapies.

How similar studies have gone: Other registries and observational studies have shown success in improving patient outcomes and treatment understanding in similar conditions, making this approach promising.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria:

* Age \<26 years old
* Current physician diagnosis of atopic dermatitis
* Provide signed informed consent if ≥ 18 years old
* Provide signed informed consent by parent or legal guardian (if \<18 years old) and informed assent if applicable
* Subject and/or parent/legal guardian is willing to be contacted in the future by study staff
* Seen for clinical care at Johns Hopkins since 1/1/2017
* Previously on, currently on, or planning to initiate (within next 6 months) a systemic AD therapy

Exclusion criteria:

* Age ≥26 years old at the time of registry enrollment
* Does not speak English
* If \<18 years old, has a primary caretaker who does not speak English
* If \<18 years old, parent/legal guardian is unwilling to sign the written informed consent
* Is a foster child
* Has not received clinical care at Johns Hopkins since 1/1/2017

Where it's running

  • Johns Hopkins University
    Baltimore, Maryland, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.