Online registry on a migraine device device during pregnancy
Follows pregnant women with migraine who may use a nerve-stimulation device.
Plain-language title generated from the registry record
Registry title: External Trigeminal Nerve Stimulation for Migraine Treatment in Pregnancy
Key facts
- Where
- Darien, United StatesSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 44 years old?
Source: NCT06788977, who can take part
Where in United States
- DarienDarien, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Cefaly Technology
- Trial code
- NCT06788977
- Record updated
- 15 April 2026
- Original description
This online registry aims to understand the potential benefits and safety of external trigeminal nerve stimulation for the treatment of migraine in pregnant women. Women do not need to use external trigeminal nerve stimulation or any other form of migraine treatment to participate in the registry.Read full original descriptionShow less
CEFALY Pregnancy Registry
This online registry aims to understand the potential benefits and safety of external trigeminal nerve stimulation for the treatment of migraine in pregnant women. Women do not need to use external trigeminal nerve stimulation or any other form of migraine treatment to participate in the registry.
The main question it aims to answer is:
Is external trigeminal nerve stimulation a safe and effective option for migraine treatment during and after pregnancy?
There are no required changes in migraine treatment to participate in this registry. Participants may or may not use external trigeminal nerve stimulation or any other treatment they currently use and may still participate in the registry. There are no clinic or research visits, as the registry is entirely online. Participants will be asked to complete up to six 15- 20-minute surveys over a time period of up to 12 months.
Inclusion: Patients willing and able to provide simple consent for registry participation; Has access to email, text messages via smartphone or computer with internet access; Be between the ages of 18 to 44 years at enrollment; Pregnant with one fetus/baby at time of enrollment (singleton pregnancy); Have headaches or migraines prior to pregnancy and continued to have headaches or migraines into pregnancy OR headaches or migraines began while pregnant in the first trimester; Able to provide proof of active intrauterine pregnancy and estimated due date, via online document upload, using any of the following documents:; ultrasound report of current pregnancy; beta hcg lab report; a signed provider's medical documentation confirming intrauterine pregnancy with fetal heart sounds and estimated due date; a signed provider's note on a prescription sheet or physician letterhead confirming intrauterine pregnancy and estimated due date.
Exclusion: Patients with any other condition which might preclude participation in the opinion of the patient's physician(s) or the study's principal investigator; Patients under the age of 18 or over the age of 44 at enrollment; Not pregnant at time of enrollment; Pregnant with more than one fetus/baby at time of enrollment (multigestational pregnancy); No access to email, smartphone, or computer with internet access.