Prader-Willi Syndrome Clinical Trial
Official title:
11 Beta Hydroxysteroid Dehydrogenase 1 (11-beta HSD 1) Activity in Patients With Prader-Willi Syndrome and in Healthy Controls
The purpose of the study is to find out if people with Prader-Willi syndrome have a difference in the protein which changes inactive cortisone to the active stress hormone cortisol.
Status | Completed |
Enrollment | 36 |
Est. completion date | August 2010 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 6 Months and older |
Eligibility |
Inclusion Criteria: - Prader-Willi syndrome confirmed by molecular testing, ages 6 months to adult - Controls: Age-matched, sex-matched, developmentally normal, BMI-controlled healthy or obese subjects Exclusion Criteria: - PWS subjects without molecular confirmation of the diagnosis - Subjects receiving glucocorticoid treatment within 3 months of evaluation - Subjects receiving growth hormone within one year prior to analysis |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
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Children's Mercy Hospital Kansas City |
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