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Clinical Trial Summary

The purpose of this study is to evaluate the contraceptive efficacy and safety of an oral contraceptive containing a combination of LNG 100mcg/EE 20mcg compared to LNG 150mcg/EE 30 mcg.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02021097
Study type Interventional
Source Regenex Pharmaceutical, China
Contact Chengliang Xiong, Dr
Email clxiong951@sina.cn
Status Recruiting
Phase Phase 3
Start date February 2012
Completion date February 2016

See also
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