Retrospective Study on the Use of CEFALY® Device During Migraine Attacks

NCT ID: NCT02616978

Last Updated: 2017-05-08

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 807 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-11-30
• Study Completion Date: 2015-12-31

Brief Summary

This is an Internet survey to collect data on the use of the Cefaly device to treat migraine attacks in regular Cefaly users.

Detailed Description

About 1000 CEFALY users, having the device since more than one year and having reordered electrodes in the last year, will be invited to participate to an Internet survey. This survey contains at most 8 questions, and data will be collected completely anonymously. Questions concern the use or not of the CEFALY during migraine attacks, the number of treated attacks and the number and type of acute anti-migraine drugs that were avoided thanks to the use of the CEFALY.

Conditions

Migraine

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: RETROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Subjects using Cefaly device regularly for more than a year identify by reordering of electrodes during the last year.
• History of likely episodic or chronic migraine with or without aura diagnosed by a physician

Exclusion Criteria

• N/A

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cefaly Technology

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

References

Penning S, Schoenen J. A survey on migraine attack treatment with the CEFALY(R) device in regular users. Acta Neurol Belg. 2017 Jun;117(2):547-549. doi: 10.1007/s13760-017-0757-z. Epub 2017 Feb 9. No abstract available.

Reference Type: RESULT

PMID: 28185179 (View on PubMed)

Other Identifiers

50214

Identifier Type: -

Identifier Source: org_study_id