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NCT04089761 · ClinicalTrials.gov registry record · NA

Safety and Efficacy of Nerivio™ for the Acute Treatment of Migraine in Adolescents

A NA study, sponsored by Theranica.

Terminated
Registry status
NA
Development phase
60
Enrollment target

NCT04089761 is a NA study that was terminated before completion, run by Theranica. The registered enrollment target is 60 participants.

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The verdict

NCT04089761, a NA study, was terminated before completion, sponsored by Theranica.

TERMINATED
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

Nerivio™ is an FDA-authorized remote electrical neuromodulation (REN) device for the acute treatment of migraine with or without aura in patients 18 years old or above who do not have 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. This is a prospective, single arm, open label, multicenter trial of the safety and efficacy of Nerivio™ for the acute treatment of migraine in adolescents The study will be conducted in three phases: Phase I - Run-in: Phase II - Treatment phase: Phase III (optional) - Free-use

Interventions

  • DEVICE Nerivio

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2019-10-01
Est. Completion 2020-05-24
Phase NA

Sponsor

Theranica

22 total trials

What the Registry Record Tells You About NCT04089761

The ClinicalTrials.gov registry entry for NCT04089761 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Theranica, which has 22 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Nerivio is the first listed.

NCT04089761 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04089761 about?

NCT04089761 is a clinical study titled "Safety and Efficacy of Nerivio™ for the Acute Treatment of Migraine in Adolescents". Nerivio™ is an FDA-authorized remote electrical neuromodulation (REN) device for the acute treatment of migraine with or without aura in patients 18 years old or above who do not have chronic migraine. The device delivers transcutaneous electrical stimulation to the upper arm to induce conditioned p...

What is the current status of trial NCT04089761?

This trial is currently terminated. It is a NA study. The enrollment target is 60 participants. The study started on 2019-10-01. Estimated completion is 2020-05-24.

What interventions are being tested in trial NCT04089761?

The interventions under investigation include: Nerivio (DEVICE).

Who is sponsoring clinical trial NCT04089761?

This trial is sponsored by Theranica, which has 22 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.