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NCT05761158 Clinical Trial

Study of the Characteristics of Pruritus in Patients With Frontal Fibrosing Alopecia or Lichen Planus Pilaris

Alopecia Clinical Trial

— PRURIT-ALOPECI  

Official title:
Study of the Characteristics of Pruritus in Patients With Frontal Fibrosing Alopecia or Lichen Planus Pilaris

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT05761158
Other study ID # 29BRC22.0227
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date March 14, 2023
Est. completion date May 25, 2023

Study information
Verified date February 2023
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The prevalence of pruritus has been studied in frontal fibrosis alopecia (FFA) and lichen planus pilaris (LPP), but there are no studies evaluating the characteristics of pruritus, the correlation between pruritus and disease activity, and its impact on quality of life. The knowledge of the characteristics of pruritus, of the link "disease activity - pruritus", and its impact on the quality of life could allow us to modify the management of the patient (modification or intensification of therapy, close monitoring...)

Recruitment information / eligibility
Status Terminated
Enrollment 21
Est. completion date May 25, 2023
Est. primary completion date May 25, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major patient. - Fibrosing frontal alopecia or lichen planus pilaris - Presence of pruritus of the scalp : a positive response to the question "do you experience itchy scalp?" - The patient received an information note and did not object to the study Exclusion Criteria: - Patients under 18 years of age. - Other pathologies causing scalp pruritus (seborrheic dermatitis, contact dermatitis, lupus, Quinquaud's decalcifying folliculitis, ectoparasitosis, scalp psoriasis, ringworm, red sclap syndrome, dermatomyositis, central centrifugal cicatricial alopecia (CCCA)) - Refusal to participate by the patient. - Patient under legal protection (curatorship, guardianship, ...) - Patient not covered by social security

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnaire
patients are asked to complete a questionnaire

Locations
Country Name City State
France CHU Brest Brest

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Study of the characteristics of pruritus in patients with frontal fibrosis alopecia or lichen planus pilaris Questionnaire of Brest Hour1
Primary Study of the characteristics of pruritus in patients with frontal fibrosis alopecia or lichen 5D itch scale Hour1
Secondary Study the relationship between disease activity (AFF or LPP) and pruritus, as well as the impact of pruritus on patients' quality of life. ItchyQol (Itchy Quality of Life) Hour1
Secondary Study the relationship between disease activity (AFF or LPP) and pruritus, as well as the impact of pruritus on patients' quality of life. Questionnaire of FFASI Hour1
Secondary Study the relationship between disease activity (AFF or LPP) and pruritus, as well as the impact of pruritus on patients' quality of life. Questionnaire of LPPAI Hour1
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