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Clinical Trial Summary

The purpose of the investigators study is to create the evidence of effectivness on climacteric syndrome in patients affected by breast cancer, by acupuncture added to the standard care (self care).


Clinical Trial Description

The study will be performed under randomized, open, controlled design. The effect of acupuncture and control group will be compared including the following outcomes: Greene climacteric scale score, quality of life (MenQol italian version), overall improvement in climacteric syndrome, adverse effects from treatment. ;


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 NCT01275807
Study type Interventional
Source Azienda Usl di Bologna
Contact
Status Completed
Phase Phase 4
Start date March 2010
Completion date September 2015

See also
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Completed NCT03118908 - Clinical Evaluation of Effectiveness and Safety of Amberen and Smart B by Women With Climacteric Syndrome N/A