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Clinical Trial Summary

To investigate if there are detectable changes in volume and circulation in breasts of healthy volunteers using toremifene 20 mg in luteal phase of the menstruation cycle versus nonmedicated cycle.


Clinical Trial Description

20 women were participated to this trial. ;


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01417754
Study type Interventional
Source Satakunta Central Hospital
Contact
Status Completed
Phase Phase 3
Start date September 2010
Completion date June 2011

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