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This is study designed to confirm the effectiveness of the Sana Device in patients with pain due to fibromyalgia on quality of life as measured by the Fibromyalgia Impact Questionnaire Revised (FIQR). It is a two arm study in which subjects will be randomly assigned to either active device group or sham-controlled group.
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166 participants in 2 patient groups
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Sinead Walsh; Melanie Maron
Data sourced from clinicaltrials.gov
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