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Comparison of Transdermal and Oral Estrogens in Adolescent Girls With Ovarian Failure
Not Recruiting
Trial ID: NCT01023178
Purpose
To directly compare the safety (by laboratory evaluation) and efficacy (feminization and growth) of three commonly used estrogen preparations in adolescent patients with ovarian failure, either due to congenital causes (Turner syndrome) or medical therapies. We hypothesize that transdermal estrogen will have equivalent efficacy and a more favorable safety profile in comparison with conventional oral estrogen replacement.
Official Title
Comparison of Transdermal and Oral Estrogens in Adolescents With Ovarian Failure
Stanford Investigator(s)
Eligibility
Inclusion Criteria: in whom initiation of estrogen therapy has been recommended due to ovarian failure
* Outpatients
* age \>=12 years to 17.99 years old
Exclusion Criteria:
* spontaneous menses
* significant concurrent medical problem including:
* Liver function tests (LFTs) 3 times normal
* clotting disorder
* ongoing cancer treatment
Intervention(s):
drug: 17beta Estradiol
drug: Conjugated estrogens
drug: 17Beta Estradiol - transdermal
drug: Progesterone, micronized
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Sejal Shah
6507235791