CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 42 enrolled
Drug / intervention
Neriviodevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04161807
NCT04161807N/ACompleted

Efficacy and Safety of Nerivio™, a Remote Electrical Neuromodulation Device, for Acute Treatment of Migraine in People With Chronic Migraine: an Open Label, Single Arm, Multicenter Study

Theranica·interventional·Posted Nov 13, 2019·Updated Feb 16, 2021

In Brief

A clinical study evaluating Nerivio for Chronic Migraine. Completed, enrolled 42 participants across 2 sites in 2 countries.

Detailed Summary

This study is intended to evaluate the efficacy and safety of Nerivio, an FDA-authorized remote electrical neuromodulation (REN) device for the acute treatment of migraine, for the acute treatment of migraine in people with chronic migraine. The device delivers transcutaneous electrical stimulation to the upper arm to induce conditioned pain modulation (CPM) that activates a descending endogenous analgesic mechanism. The study duration consists of a 4 weeks of active treatment with the device in about 40 patients.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIsrael, United States
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedNov 13, 2019
Enrollment StartSep 18, 2019
Primary CompletionFeb 18, 2020
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 6.6 years ago

Interventions

Neriviodevice

The device delivers transcutaneous electrical stimulation to the upper arm to induce conditioned pain modulation (CPM) that activates a descending endogenous analgesic mechanism. The treatment is self-administered and controlled by a smartphone application.