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.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | CorEvitas Research network |
| Locations | 1 site (Waltham, Massachusetts) |
| Status | Recruiting |
| Started | July 21, 2026 |
| Main results expected | December 31, 2099 |
| Study ends | December 31, 2099 |
| Registry record updated | August 26, 2026 |
| Trial ID | NCT07598058 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
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CorEvitas, LLC
Waltham, Massachusetts, United States Recruiting
Study contacts
- Study coordinator: Chronic Hand Eczema Registry Team
- Email: CHEregistry@thermofisher.com
- Phone: +1 508 408 5531
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.