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NCT03076515

Migraine Treatment With Nerivio Migra Neurostimulation Device

Terminated NA Results posted Last updated 17 July 2025
What this trial tests

NA trial testing Nerivio Migra neurostimulation in Acute Migraine in 120 participants. Terminated before completion.

Timeline
2 April 2017
Primary endpoint
31 January 2018
1 April 2018

Quick facts

Lead sponsorTheranica
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment120
Start date2 April 2017
Primary completion31 January 2018
Estimated completion1 April 2018
Sites8 locations across United States, Israel

Drugs / interventions tested

Conditions studied

Sponsor

Theranica — full company profile →

Who can join

Adults 18 to 75, any sex, with Acute Migraine. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Percentage of Participants With Pain Relief 2 Hours Post Treatment Primary · 2 hours post treatment

Percentage of participants reporting pain relief from pain (pain reduction from 3 or 2 to 1 or 0 or pain reduction from 1 to 0) 2 hours post treatment without rescue medications in at least 50% of treated attacks

GroupValue95% CI
Nerivio Migra Active36.3
Nerivio Migra Placebo27.2

Sponsor's own description

This is a prospective, randomized, double-blind, sham controlled multi-center trial. Ratio between treatment and control groups will be 1:1, stratified by center and use of preventive medications.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Theranica trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03076515.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing