Expired Study
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Norfolk, Virginia 23507


Purpose:

Estradiol treatment is effective at reducing vasomotor symptoms (eg, hot flushes) in postmenopausal women. Vivus has a proprietary spray delivery system (Evamist) for estradiol. This study will evaluate the safety and efficacy of this product.


Study summary:

This is a multicenter, randomized, double-blind, placebo-controlled trial evaluating different doses of transdermal estradiol delivered by spray to symptomatic postmenopausal women. The endpoints are the reduction in frequency and severity of hot flushes.


Criteria:

Inclusion Criteria: - Postmenopausal women - Ages 35 or older - Frequent moderate to severe hot flushes - Qualifying general medical health Exclusion Criteria: - Disqualifying gynecological disorders - Disqualifying dermatological disorders - Disqualifying concurrent conditions


NCT ID:

NCT00122200


Primary Contact:

Study Director
Sam Teichman, MD
Vivus Clinical Research Department


Backup Contact:

N/A


Location Contact:

Norfolk, Virginia 23507
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

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