UnknownNot Applicable

A Study to Characterize Epidemiology, Clinical and Genetic Features of Kallmann Syndrome in Finland

Finland50 participantsStarted 2007-12

Plain-language summary

Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.

Age range15 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Kallmann syndrome * Age 15 yrs or more Exclusion Criteria: * Severe mental retardation

Clinical features including quality of life, reversibility and genetic features of Kallmann syndrome in Finland

Timeframe: 0, 3 mo and during subsequent F/U

NCT IDNCT00623116

SponsorHospital for Children and Adolescents, Finland

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2012-12