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

NAEnrolling by invitationINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

December 31, 2007

Primary Completion Date

December 31, 2012

Study Completion Date

December 31, 2025

Conditions
Kallmann Syndrome
Interventions
DRUG

Short withdrawal of testosterone, gonadotropins or estrogenic compounds (see below)

clinical examination, biochemical profile, and genetic characterization. Possibility to stop hormone therapy with drugs containing testosterone (Atmos®, Testim®, Testogel®, Nebido®, Panteston®, Sustanon®), FSH (Gonal-F®, Puregon®), hCG (Pregnyl®), estrogenic compounds (such as Estrofem®, Divigel®, Estrena®, Climara®, Estradot®, Evorel®, Femseven®: Merimono®, Progynova®, Ovestin®, Zumenon®, Estrogel®, Femoston®, Femoston combi®, Divina®, Divitren®, Indivina®, Estalis sekvens®, Evorel sequi®, Novofem®, Trisekvens®, Activelle®, Estalis®, Evorel conti®, Kliogest®, Mericomb®, Mericomb Mite®, Merigest®: Angeliq®) for 3 mo to assess reversibility of GnRH-deficiency will be offered.

Trial Locations (1)

00029 HUCH

Hospital for Children and Adolescents, Helsinki University Central Hospital, Helsinki

All Listed Sponsors
lead

Hospital for Children and Adolescents, Finland

OTHER