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

Study Status: Enrolling by invitation
Recruit Status: Enrolling by invitation
Study Type: Interventional

Official Title: Kallmann Syndrome in Finland

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

Detailed Summary: Kallmann syndrome is comprised of idiopathic hypogonadotropic hypogonadism and anosmia (inability to smell). Associated phenotypes may include cryptorchidism, microphallus, bone deformations, mirror movements, hearing loss and infertility. Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.
Sponsor: Hospital for Children and Adolescents, Finland

Current Primary Outcome: Clinical features including quality of life, reversibility and genetic features of Kallmann syndrome in Finland [ Time Frame: 0, 3 mo and during subsequent F/U ]

Original Primary Outcome: Same as current

Current Secondary Outcome: epidemiology [ Time Frame: by 2012 (anticipated) ]

Original Secondary Outcome: Same as current

Information By: Hospital for Children and Adolescents, Finland

Dates:
Date Received: January 11, 2008
Date Started: December 2007
Date Completion: December 2025
Last Updated: February 13, 2008
Last Verified: January 2008