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Evaluation of the Efficacy of Systemic Treatments for Alopecia (ESTAA)

Active, not recruiting
Conditions
Alopecia Areata
Registration Number
NCT06471114
Lead Sponsor
University Hospital, Brest
Brief Summary

The aim of our study was to retrospectively assess the efficacy and safety of systemic treatments in patients with alopecia areata, by recruiting cases from the HUGO network (H么pitaux Universitaires du Grand Ouest), a network of 5 hospitals : Brest, Nantes, Rennes, Angers and Tours.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
250
Inclusion Criteria
  • Patient with severe alopecia
  • Has received at least one systemic treatment for at least 3 months (among methotrexate, intravenous or oral corticosteroid therapy, Ciclosporin, UVA/UVB phototherapy)
  • Patient affiliated to a social security scheme
  • Age greater than or equal to 18 years
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Exclusion Criteria
  • Patients under legal protection (guardianship, curatorship, etc.)
  • Refusal to participate
  • Other cause of alopecia
  • Follow-up less than 3 months
  • Age under 18 years
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Short-term efficacy and security of systemic treatmentsFrom January 2010 to December 2020

Response rates including complete response or partial response or no response for each modality of treatment. and Side effects rate

Secondary Outcome Measures
NameTimeMethod
Long-term efficacy of systemic treatmentsFrom January 2010 to December 2020

Among responders (CR and PR), the maintained response rate and relapse rate

Trial Locations

Locations (1)

Chu Brest

馃嚝馃嚪

Brest, France

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