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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01689805
Other study ID # FLG-255-AR
Secondary ID
Status Recruiting
Phase N/A
First received June 23, 2011
Last updated September 18, 2012
Start date June 2011

Study information

Verified date September 2012
Source Helsinki University Central Hospital
Contact Anita Remitz, MD, PhD
Phone +358-9-4711
Email anita.remitz@hus.fi
Is FDA regulated No
Health authority Finland: Ministry of Social Affairs and Health
Study type Observational

Clinical Trial Summary

Atopic dermatitis is a common disease which affects about one million people in Finland at some stage of their life. In atopic dermatitis we see a superficial inflammation of the skin and a defect in skin barrier function. The filaggrin protein plays a central role in the skin barrier function and studies indicate that about 30% of patients with atopic dermatitis have a mutation in the filaggrin gene. The aim of the study is to investigate whether a mutation in the filaggrin gene affects the clinical treatment outcome in patients with atopic dermatitis. If a mutation predisposes to a worse response to treatment, this could be examined and those patients with the mutation could be given extra treatment support for their atopic dermatitis. The prevalence of filaggrin mutation in the Finnish non-atopic population is studied in the control group.


Recruitment information / eligibility

Status Recruiting
Enrollment 800
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria (patients with atopic dermatitis):

- Age at least 18 years

- Clinical diagnosis of atopic dermatitis

- Need for follow-up at the Skin and Allergy Hospital

- Patient gives signed informed consent to participate in this study

- Patients parents and grandparents are of Finnish origin

Inclusion Criteria (Controls):

- No history of atopy or skin disease

- Age at least 18 years

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Finland Skin and Allergy Hospital, Departments of Dermatology and Clinical Genetics Helsinki

Sponsors (1)

Lead Sponsor Collaborator
Helsinki University Central Hospital

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Filaggrin mutation No
Secondary Response to treatment 12 months No
Secondary Serum IgE 12 months No
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