drugset / Trial / NCT03401047

Study to Assess Potential Impairments in Estradiol Augmentation of Gonadotropin Secretion in Polycystic Ovary Syndrome

NCT03401047

Phase 0 Recruiting 37 enrolled University of Virginia
NaSingle-groupOpen-labelBasic science

Summary

The purpose of this study is to determine if estradiol augmentation of luteinizing hormone (LH) secretion secretion (primary endpoint) and follicle-stimulating hormone (FSH) secretion (secondary endpoint) is reduced in adult women with polycystic ovary syndrome.

Timeline

Start
2017-11-30
Primary completion
2025-10-01
Completion
2025-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Estradiol Other / unclassified 0.1 mg Other
Subject Estradiol Other / unclassified 0.6 mg Other