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Clinical Trial Summary

The purpose of this study is to determine whether ovaria comp. is effective in relieving climacteric symptoms.


Clinical Trial Description

Complementary treatments for climacteric symptoms are used by many women although their efficacy and safety is mostly unproven.

The use of the complex homeopathic remedy Ovaria comp. for the relief of climacteric symptoms will be examined in this three-armed intervention trial and measured with the menopause rating scale II before and after each study phase of 12 weeks. Participants will receive the verum during two treatment phases of 12 weeks and the placebo during one treatment phase of 12 weeks in different sequences and are stratified for post- and perimenopausal status. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00152776
Study type Interventional
Source Heidelberg University
Contact
Status Completed
Phase Phase 4
Start date February 2005
Completion date December 2006

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