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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT00623116 |
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Date of registration:
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11/01/2008 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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A Study to Characterize Epidemiology, Clinical and Genetic Features of Kallmann Syndrome in Finland
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Scientific title:
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Kallmann Syndrome in Finland |
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Date of first enrolment:
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December 2007 |
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Target sample size:
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50 |
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Recruitment status: |
Enrolling by invitation |
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URL:
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http://clinicaltrials.gov/show/NCT00623116 |
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Study type:
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Interventional |
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Study design:
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Finland
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Contacts
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Name:
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Taneli J Raivio, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Hospital for Children and Adolescents, Helsinki University Central Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Kallmann syndrome
- Age 15 yrs or more
Exclusion Criteria:
- Severe mental retardation
Age minimum:
15 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Kallmann Syndrome
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Intervention(s)
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Drug: Short withdrawal of testosterone, gonadotropins or estrogenic compounds (see below)
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Primary Outcome(s)
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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]
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Secondary Outcome(s)
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epidemiology
[Time Frame: by 2012 (anticipated)]
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Secondary ID(s)
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231408
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286/E7/2007
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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