Clinical trial Recruiting at 1 site Observational Ages 18 and up

Chronic Hand Eczema Patient Registry for Drug Safety and Effectiveness

Official title: PPDTM CorEvitasTM Chronic Hand Eczema (CHE) Drug Safety and Effectiveness Registry

Run by CorEvitas · NCT07598058 · Data updated 2026-11-12

This registry follows adults with chronic hand eczema to see how real-world treatments work and how safe they are over time under their normal dermatology care.

More Chronic Hand Eczema trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment2000 (estimated)
SponsorCorEvitas
Research network
Locations1 site (Waltham, Massachusetts)
StatusRecruiting
StartedJuly 21, 2026
Main results expectedDecember 31, 2099
Study endsDecember 31, 2099
Registry record updatedAugust 26, 2026
Trial IDNCT07598058 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with moderate-to-severe chronic hand eczema starting an eligible therapy, willing to consent and complete electronic forms.

Probably not a fit

Patients who do not receive a response from providers or who discontinue treatment early may not derive direct benefit from the registry data.

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

What this trial studies

This is a prospective, observational registry enrolling adults with moderate-to-severe chronic hand eczema who are starting an eligible medication. Data are collected from patients and their treating providers during routine visits using standardized forms. The goal is to study long-term real-world safety and effectiveness of standard treatments, describe the disease course, and inform decision-making for patients, clinicians, and regulators. The registry may address multiple research questions and support risk–benefit evaluations by manufacturers and regulators. Participation relies on electronic data capture and ongoing consent.

Why it matters

Potential benefit: Participants may contribute to knowledge that improves understanding of how CHE therapies perform in real-world practice, potentially guiding future treatment decisions.

How similar studies have gone: Observational CHE registries have provided real-world safety and effectiveness insights, though results can be context-specific to treatments and populations.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* To be eligible to participate in this registry, an individual must meet all of the following criteria:

  1. Diagnosed with moderate-to-severe CHE by a dermatologist or other qualified healthcare provider at the time of enrollment and initiating an eligible medication.
  2. Is at least 18 years of age or older and has attained the legal age for consent to procedures involved in the research, under the applicable law of the jurisdiction in which the research is being conducted at the time of enrollment
  3. Is willing and able to consent to participation in the registry
  4. Is willing and able to complete registry-related forms electronically via personal devices.
  5. Is willing and able to provide the information (first name, last name, email address, language and primary time zone) required to create an account to allow you to complete registry forms via a personal device;
  6. Is willing and able to provide Personal Information (full legal name, sex, date of birth, home address zip or postal code and email address or phone number at a minimum) if required based on registry location and applicable laws and regulations.

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in the registry:

1\) Is participating or planning to participate in a blinded clinical trial for a CHE drug

Where it's running

  • CorEvitas, LLC
    Waltham, Massachusetts, 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.