Effectiveness of the Sana Device on Fibromyalgia Symptoms

Status Not yet recruiting

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05394610
Study type	Interventional
Source	Sana Health
Contact	Melanie Maron
Phone	2157461419
Email	fibromyalgiastudy@pennmedicine.upenn.edu
Status	Not yet recruiting
Phase	N/A
Start date	June 2024
Completion date	June 2025

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