Status:

ENROLLING_BY_INVITATION

CorEvitas Atopic Dermatitis Registry: a Study of Post Approval Drug Safety and Effectiveness

Lead Sponsor:

CorEvitas

Conditions:

Atopic Dermatitis

Eligibility:

All Genders

18+ years

Brief Summary

This prospective, non-interventional research registry is designed to study the comparative effectiveness and comparative safety of approved treatments for patients with atopic dermatitis under the ca...

Detailed Description

The objective of the CorEvitas Atopic Dermatitis (AD) Registry is to create a national cohort of patients with atopic dermatitis. Data collected will be used to extensively evaluate the effectiveness ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria Has been diagnosed with AD by a dermatologist or qualified dermatology provider.
  • 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.
  • 3\) Willing and able to provide consent for participation in the registry. 4) Willing and able to provide Personal Information (full legal name, sex, date of birth, home address zip/postal code, and email address OR phone number at a minimum) if required based on registry location and applicable laws and regulations. 5) Has been prescribed a new Enrollment Eligible Medication. A new therapy is a medication that the subject has never taken before.
  • At the time of registry enrollment OR
  • Within 12 months prior to registry enrollment
  • Exclusion Criteria:
  • 1)Is participating or planning to participate in a blinded clinical trial for an AD drug.
  • Follow-Up Criteria
  • Registry Follow-Up data collection should be done at the time of routine clinical encounters approximately every 6 months. Routine or standard of care clinical encounters may occur in between two registry visits, but the data collected in the Follow-Up forms should cover the time period since the last registry visit.
  • For planning purposes, each Follow-Up visit is anchored to the date of the last eligible registry visit. A Follow-Up visit is eligible for payment if 150 days have passed since the last visit submission. A Follow-Up visit is not eligible for payment if conducted less than 150 days since the last registry visits except when the EARLY Follow-Up visit Criteria are satisfied.
  • EARLY Follow-Up Criteria
  • A registry Follow-Up visit should be conducted whenever a patient is prescribed or receiving the first dose of a new Eligible Medication even if less than 150 days have passed since the last registry visit. When the EARLY Follow-Up criteria are met, the next anticipated registry visit is calculated from the date of the Early Follow-Up visit.

Exclusion

    Key Trial Info

    Start Date :

    July 14 2020

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    December 1 2100

    Estimated Enrollment :

    10000 Patients enrolled

    Trial Details

    Trial ID

    NCT04504955

    Start Date

    July 14 2020

    End Date

    December 1 2100

    Last Update

    December 4 2024

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    CorEvitas, LLC

    Waltham, Massachusetts, United States, 02451