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Clinical Trial Summary

To assess potential benefits associated with both intermittent (use for 3 weeks, remove for 1 week, as defined in the package insert) and continuous (use for 4 weeks, then replace) CVR use among women either with BV or at high risk for BV. The investigators will also recruit women who are HSV2-infected.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02432404
Study type Interventional
Source University of Washington
Contact
Status Completed
Phase Phase 4
Start date March 2016
Completion date November 2021

See also
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