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Vaginitis clinical trials

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NCT ID: NCT02460302 Withdrawn - Menopause Clinical Trials

Vaginal Progesterone Versus Placebo for the Treatment of Vaginal Atrophy

Start date: December 2016
Phase: Phase 2
Study type: Interventional

Atrophic vaginitis affects the majority of post-menopausal women. It is characterized by dryness and inflammation of the vagina, with thinning of the vaginal tissues. Atrophic vaginitis is caused by the decreased effect of estrogens post menopause. Traditionally, local estrogens have been used to treat atrophic vaginitis Studies have shown that there are progesterone receptors in vaginal tissues. The use of progesterone to treat atrophic vaginitis has not yet been studied. However, its use has been studied in other populations including as a fertility medication in pregnant women. There is a significant group of women who cannot use, choose not to use, or do not respond to estrogenic therapies. The goal of this study is to evaluate the efficacy of vaginal progesterone in the treatment of urogenital atrophy, compared to placebo. This study is a randomized, double-blind, placebo controlled trial. The ultimate goal is to expand the treatment options for patients with symptoms of vaginal atrophy.

NCT ID: NCT02316249 Withdrawn - Vaginitis Clinical Trials

Vaginal Creams to Reduce Vaginal Erosion in Pessary Users

Start date: April 2015
Phase: Phase 2
Study type: Interventional

To compare the use of Estrace ® vaginal cream against a placebo vaginal cream in reducing symptomatic vaginal discharge and vaginal erosion in patients who are using the Gellhorn or Ring with support pessaries.