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Clinical Trial Summary

This study is conducted in Europe. The primary aim of this observational study is to investigate the occurrence of bleeding in women taking 0.5 mg estradiol and 0.1 mg norethisterone acetate (NETA) for 12 months.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01076621
Study type Observational
Source Novo Nordisk A/S
Contact
Status Completed
Phase N/A
Start date May 2010
Completion date June 2013

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