A Study of Remote Electrical Neuromodulation for Acute Procedural Pain
Reason given: Enough data was collected to demonstrate device efficacy at interim analysis
Key facts
- Where
- Scottsdale, United StatesSee the site
Where in United States
- Mayo Clinic in ArizonaScottsdale, United StatesNo longer taking part
Trial details
- Who runs it
- Mayo Clinic
- Trial code
- NCT05730556
- Record updated
- 27 October 2025
- Original description
The purpose of this study is to assess the effectiveness of using remote electrical neuromodulation, using the Nerivio ® device, to relieve pain associated with receiving onabotulinumtoxinA (Botox) injections for chronic migraine prevention.Read full original descriptionShow less
Remote Electrical Neuromodulation for Acute Procedural Pain in Chronic Migraine Patients Receiving onabotulinumtoxinA
The purpose of this study is to assess the effectiveness of using remote electrical neuromodulation, using the Nerivio ® device, to relieve pain associated with receiving onabotulinumtoxinA (Botox) injections for chronic migraine prevention.
Inclusion: Meet the criteria for 1.3 chronic migraine based on ICHD3 criteria; Currently receiving onabotulinumtoxinA per PREEMPT protocol for the treatment of chronic migraine; Patient is willing and able to comply with the protocol to the satisfaction of the investigator; Patient has the capacity to provide written, informed consent for themselves.
Exclusion: Participants who have previous experience with the device; Patients with cranial deformities, prior cranial surgeries with violation of the calvarium, or shunt placement; Patients receiving concurrent nerve blocks or trigger point injections within the same visit; Participants with an active implanted electrical and/or neurostimulator device (e.g., cardiac pacemaker, cochlear implant); Participants with congestive heart failure (CHF), severe cardiac or cerebrovascular disease; Participants with uncontrolled epilepsy; Pregnant, trying to get pregnant or breastfeeding female participants; Subjects participating in any other interventional clinical study; Participants with other significant pain, medical or psychological problems that in the opinion of the investigator may confound the study assessments.