Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Toledo Health Science Campus
This study will evaluate the efficacy of the Fisher Wallace Cranial Stimulator in persons with chronic migraine who have not achieved satisfactory pain control on their current medications.
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subjects satisfying the IHS (International Headache Society) criteria for migraine
Subjects have not achieved satisfactory pain control on their current medication
Ability to maintain a daily headache diary
Stable medication use related to migraine for at least 4 weeks prior to enrollment in the study
You may not be if
Previous exposure to or experience with cranial electrotherapy stimulation (CES)
Contraindications to Fisher Wallace stimulator, such as cardiac pacemakers or implantable defibrillators, known or suspected heart disease, or pregnancy
