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Efficacy and Safety of Nerivio for the Acute Treatment of Menstrual Migraine

Retrospective, Observational Survey Study to Assess the Efficacy and Safety of Nerivio for the Acute Treatment of Menstrual Migraine

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04600388
Enrollment
121
Registered
2020-10-23
Start date
2020-09-09
Completion date
2020-11-10
Last updated
2020-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menstrual Migraine

Brief summary

Post-marketing, retrospective, observational survey study. Users (menstruating women only) of Nerivio who have used Nerivio at least 4 times between October 2019 and December 2020 will be contacted by email and/or through an app notification and will be asked to complete a 5-minute online anonymous survey assessing satisfaction, effectiveness, and safety. Eligible users will sign an informed consent form (the consent language will appear as the first page of the survey, and participants will click either agree or disagree to the consent statement; those who click agree will proceed to the survey, those who click disagree will be brought to an exit page) and complete a survey asking about their satisfaction with Nerivio and the effectiveness and safety of the device for acute treatment of menstrual migraine. During the survey, participants will be screened to verify that they have menstrual migraine (self-reported) and have used Nerivio to treat menstrual migraines.

Detailed description

This study aims to evaluate the safety and efficacy of Nerivio for the acute treatment of menstrual migraine (pure menstrual migraine or menstrually-related migraine). Up to 500 US-based adults aged 18-55 years old who have been prescribed the Nerivio device and have used it at least 4 times between October 2019 and December 2020. Informed consent must be obtained from the participant before any protocol-related activities are performed. The consent language will appear as the first page of the survey, and participants will click either agree or disagree to the consent statement; those who click agree will proceed to the survey, those who click disagree will be brought to an exit page. Users of Nerivio whose details are in the sponsor's database will be contacted by email (provided by the patient during the sign-up process in the Nerivio app required to use the device) and/or through an app notification and will be asked to complete a 5-minute online survey assessing satisfaction, effectiveness, and safety. Participants will sign an informed consent form which will appear as the first page of the survey using open-ended questions, multiple choice questions and Likert scales. Participants will be directed to provide honest opinions regarding the device use for menstrual migraine. No additional information will be collected, and no medical records will be used in this investigation.

Interventions

DEVICENerivio

Nerivio Remote Electrical Neuromodulation (REN) device

Sponsors

Theranica
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

1. Women aged 18-55 years 2. Participants have used Nerivio at least 4 times 3. Participants experience menstrual migraines (pure menstrual migraine or menstrually-related migraine; self-reported) 4. Participants have used Nerivio to treat menstrual migraine

Exclusion criteria

1\. Non-menstruating women

Design outcomes

Primary

MeasureTime frameDescription
Efficacy of Nerivio during menstrual migraines3 monthsEfficacy of Nerivio for headache relief during menstrual migraines rated on a 5-point Likert scale (1 - Not at all effective, 2 - Slightly effective, 3 - Moderately effective, 4 - Very effective, 5- Extremely effective)
Satisfection of using Nerivio during menstrual migraines3 monthsSatisfection of using Nerivio during menstrual migraines rated on a 5-point Likert scale )1 - Not at all satisfied, 2 - Slightly dissatisfied, 3 - Neutral, 4 - Slightly satisfied, 5 -Extremely satisfied)

Secondary

MeasureTime frameDescription
Mean headache relief3 monthsMean percentage of menstrual migraine attacks in which relief was achieved
Medication consumption3 monthsPercentage of menstrual migraine attacks in which acute medication was avoided following using the Nerivio
Reduction of menstrual cramps3 monthsPercentage of patients reports reduction in menstrual cramps following using of Nerivio

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026