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Clinical Trial Summary

This study aims to understand the efficacy of two probiotic interventions as prophylaxes of fibromyalgia symptoms in individuals diagnosed.

The primary outcome measure will be the progression and treatment of fibromyalgia, defined as a decrease in the Fibromyalgia Impact Questionnaire (FIQ) score, other otucomes will be the effect on the symptoms of anxiety and depression associated with fibromyalgia, defined as a decrease in the Hospital Anxiety and Depression Scale (HAD) score; perception of pain by scoring on a Visual Analogical Pain Scale (VAS), and differences in the patient's usual medical treatment. Finally adverse effects will be evaluated.

The study will have two arms: one arm including a probiotic preparation and a placebo arm.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04435886
Study type Interventional
Source Biopolis S.L.
Contact María Empar Chenoll, PhD
Phone +34 673 53 53 44
Email maria.chenoll@adm.com
Status Recruiting
Phase N/A
Start date March 2, 2020
Completion date May 2, 2021

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