Fibromyalgia Clinical Trial
Official title:
A 12-weeks Prospective, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effect of a Probiotic in the Treatment of Fibromyalgia
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.
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