Vagus Nerve Stimulation(VNS) As Treatment For Fibromyalgia Patients

The main goal of this study is to generate preliminary data on the effect of VNS on FM symptoms. Specifically, the investigators will utilize a recently developed, non-invasive method of tVNS (transcutaneous VNS) via auricular branches of vagus nerve (ABVN). The investigators plan to conduct an 4-week clinical study with 60 subjects randomized into 2 groups(tVNS group and control group; 30 subjects in each group). The primary outcome measure will be pain intensity. The secondary outcome measures will be fatigue, sleep, and other health-related quality of life measure. These outcome measures will be made at baseline week 0 (before any intervention), and at the end of 4 weeks.

Inclusion criteria

• Subject is 18 to 80 years old, including both male and female subjects.
• Subject has a documented diagnosis of FM for at least three months. This requirement is to avoid the uncertainty of an unstable pain condition and to minimize the study variation.
• Subject has a pain score of 4 or above (numeric pain score: 0 - 10 from no pain to worst pain).

Exclusion criteria

• Subject has current cardiac arrhythmia or had implanted cardiac pacemaker or AICD device.
• Subject has major psychiatric disorder required hospitalization in the last 3 months.
• Subject has active infection at the site of device application.
• Subject has recurrent syncope symptoms within the past three months.
• Subject is pregnant.
• Subject has had VNS treatment within the past two months.

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