Actively Recruiting

Age: 16Years +
All Genders
ID06283316

Systemic Treatments for Alopecia Areata Registry

Led by Erasmus Medical Center · Updated on 2024-02-28

10000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to collect and analyze information on systemic treatments used for alopecia areata, a condition that causes hair loss and affects patients' quality of life. It focuses on patients with moderate-to-severe forms of alopecia areata who need more extensive treatments beyond localized therapies. The study is a long-term, multicenter, prospective, observational registry designed to gather real-world data on how these treatments work and their safety over time. Patients who have alopecia areata and are starting or currently using systemic treatments are included in this registry. The study does not assign any treatments but observes the outcomes as patients receive their prescribed therapies in routine clinical care. Data collection occurs at regular intervals of every 3 to 6 months, and the registry plans to follow each participant for at least 10 years to assess the long-term effectiveness and safety of these treatments. Participants will be involved in providing information through clinical assessments, including the Severity of Alopecia Tool (SALT) score, the Dermatology Life Quality Index (DLQI), and the Alopecia Areata Symptom Impact Scale (AASIS). These evaluations, along with epidemiological data, will be collected at baseline and throughout the follow-up period. Researchers will monitor treatment outcomes, quality of life impacts, and safety over the extended observation time to better understand systemic therapies for alopecia areata.

CONDITIONS

Brief Title

Systemic Treatments for Alopecia Areata Registry

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with alopecia areata
  • Starting or using a systemic treatment for alopecia areata
  • Provided informed consent for registry participation
Not Eligible

You will not qualify if you...

  • Not sufficiently capable of understanding the Dutch language
  • Not willing to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - A minimum of 10 years from last patient enrolled

Participants who undergo routine care are observed to assess the effectiveness and safety of systemic treatments for alopecia areata over a long period.

Visits every 3 to 6 months

Trial Site Locations

Total: 1 location

1

Erasmus University Medical Center

Rotterdam, Netherlands

Actively Recruiting

Loading map...

Research Team

D

DirkJan Hijnen, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

A Biospecimen Collection Study to Identify the Targets of Di...

Autoimmune Diseases

Actively Recruiting

12 locations

An Exploratory Clinical Study of the Safety and Efficacy of ...

Autoimmune Diseases

Actively Recruiting

2 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here