Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Diagnosed with alopecia areata
- Starting or using a systemic treatment for alopecia areata
- Provided informed consent for registry participation
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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