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The Epidemiology, Management and Comorbidities in Alopecia Areata in Czech Republic

F

Faculty Hospital Kralovske Vinohrady

Status

Completed

Conditions

Diabetes Mellitus, Type 1
Vitiligo
Down Syndrome
Alopecia Totalis
Autoimmune Hyperthyroidism
Infections
Alopecia Areata
Atopic Rhinitis
Alopecia Areata (& Ophiasis)
Multiple Sclerosis
Atopic Asthma
Alopecia Barbae
Anemia, Pernicious
Ankylosing Spondylitis
Crohn Disease
COVID-19 Pandemic
Psoriasis
Alopecia Diffuse
Vaccine Reaction
Alopecia Universalis
Autoimmune Diseases
Atopic Dermatitis
Ulcerative Colitis
Inflammatory Bowel Diseases
Autoimmune Hypothyroidism
Lupus Erythematosus
Rheumatoid Arthritis

Treatments

Other: Exposure of interest

Study type

Observational

Funder types

Other

Identifiers

NCT05098600
NKS1001

Details and patient eligibility

About

The study series consists of three studies with the aim to assess the incidence, prevalence, risk factors, comorbidities and management of patients with alopecia areata in Czech Republic based on the patients and registry of a dermatology clinic of a metropolitan hospital.

Full description

The first study will aim to identify the incidence and prevalence of alopecia areata in the dermatology clinic of a metropolitan teaching hospital between 1/1/2011 and 31/12/2020

The second study will assess (1) the epidemiology of autoimmune and atopic diseases in patients with alopecia areata, (2) the presence of possible risk factors responsible for the onset/relapse/exacerbation of alopecia areata, (3) the levels of vitamin D and various autoantibodies,particularly thyroid autoantibodies and (4) the variety, duration, efficacy and safety profile of treatment modalities used in our hospital for the management of alopecia areata from 15/10/2021 to 14/10/2022.

The third study will monitor the monthly oscillations of vitamin D and thyroid-autoantibodies of patients with new-onset/relasping or exacerbating alopecia areata for six months, between 15/10/2021-14/10/2022 in order to observe if changes in levels of vitamin D and thyroid-antiantibodies are associated with severity and prognosis (worsening or improvement) of alopecia areata

Enrollment

123 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients visiting our clinic with a dermatologic condition between 1/1/2011-31/12/2020
  • For the second study, only patients with histologic/dermatoscopic diagnosis of new-onset/relapsing/peristent-untreated alopecia areata, presenting to our clinic between 15/10/2021-14/10/2022 are included.

Exclusion criteria

  • For the second study patients with other alopecias, patients denying data sharing despite signing the informed concent and presenting outside the study period are excluded.
  • For the third study, patients with other types of alopecia, as well as those who signed the informed consent but refused to share their data or undergo blood tests at our hospital, and those who did not visit our outpatient department at least once a month for the required duration, were excluded.

Trial design

123 participants in 1 patient group

Cases
Description:
Patients with a confirmed histologic/dermatoscopic diagnosis of Alopecia areata within the study period will be included for analysis.
Treatment:
Other: Exposure of interest

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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