RECRUITING

CorEvitas Alopecia Areata (AA) Safety and Effectiveness Registry

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Prospective, observational cohort study for subjects with AA under the care of a dermatology provider. Approximately 5,000 subjects and 100 clinical sites in North America will be recruited to participate with no defined upper limit for either target.

Official Title

CorEvitas Alopecia Areata (AA) Safety and Effectiveness Registry

Quick Facts

Study Start:2022-10-25
Study Completion:2099-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05745389

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * A subject must meet all the following criteria to participate in the registry:
  2. 1. Has been diagnosed with alopecia areata by a dermatologist or a qualified dermatology practitioner.
  3. 2. Is at least 18 years of age or older.
  4. 3. Is willing to provide Personal Information.
  5. 4. Is prescribed or starting an Enrollment Eligible Medication at the time of enrollment.
  1. * Any of the following would exclude the subject from participating in the registry:
  2. 1. Is participating or planning to participate in a double-blind randomized trial for an AA drug. Note:

Contacts and Locations

Study Contact

Cathy Cheney
CONTACT
(508) 408-5435
corevitasregistrytrials@corevitas.com
Resham Sanzagiri
CONTACT
508-948-0898
regulatory@corevitas.com

Study Locations (Sites)

CorEvitas, LLC
Waltham, Massachusetts, 02451
United States

Collaborators and Investigators

Sponsor: CorEvitas

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-10-25
Study Completion Date2099-12-31

Study Record Updates

Study Start Date2022-10-25
Study Completion Date2099-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Alopecia Areata