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Clinical Trial Summary

To evaluate user satisfaction in young nulliparous and parous women (18-29 years of age [inclusive]), using LCS16 compared to a COC over a period of 12 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03074045
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date March 13, 2017
Completion date August 5, 2022

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