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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01023178
Study type Interventional
Source Stanford University
Contact
Status Completed
Phase N/A
Start date February 2007
Completion date June 2013

See also
  Status Clinical Trial Phase
Terminated NCT02780791 - Maturation of Follicles After Transplantation of Ovarian Tissue Into the Pelvic Wall and the Ovary N/A
Completed NCT00471731 - Dry Eye in Women With Turner Syndrome and Women With Premature Ovarian Failure N/A
Enrolling by invitation NCT04009473 - Stem Cell Therapy and Growth Factor Ovarian in Vitro Activation Phase 1/Phase 2
Recruiting NCT04031456 - Autologous PRP Infusion May Restore Ovarian Function and May Promote Folliculogenesis in POI Patients Phase 2/Phase 3
Completed NCT05443282 - Ovarian Reserve and Matrix Metalloproteinases