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NCT00901953 Clinical Trial

Vestibular System in Migrainous Vertigo Patients

Migraine Disorders Clinical Trial

Official title:
Do Migrainous Vertigo Patients Have More Hypersensitivity in Their Vestibular System Than Migraine Patients Without Vertigo?

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT00901953
Other study ID # 2.2006.3376
Secondary ID
Status Enrolling by invitation
Phase N/A
First received May 12, 2009
Last updated May 14, 2009
Start date May 2007
Est. completion date September 2009

Study information
Verified date May 2009
Source University of Bergen
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Social Science Data ServicesNorway:National Committee for Medical and Health Research Ethics
Study type Observational

Clinical Trial Summary

Do migrainous vertigo patients have more pathology in their vestibular system than migraine patients without vertigo?

The aim of this study is to compare the vestibular system of migraine patients with and without vertigo in the symptom-free period by vestibular function tests, videonystagmography, vestibular evoked myogenic potentials, and subjective visual vertical.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 65
Est. completion date September 2009
Est. primary completion date May 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 16 Years to 61 Years
Eligibility Inclusion Criteria:

- migraine according to IHS criteria

- migrainous vertigo according to the Neuhauser-criteria

Exclusion Criteria:

- no history of other neurological, vestibular, opthalmologic and ENT disorders

- no medications that could possibly influence test results

- intact hearing measured by audiometry

- pregnancy

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Norway Dept. of neurology, Sørlandet Hospital HF Kristiansand

Sponsors (2)
Lead Sponsor Collaborator
University of Bergen Sorlandet Hospital HF

Country where clinical trial is conducted

Norway, 

Outcome
Type Measure Description Time frame Safety issue
Primary Differences in vestibular function Symptomfree interval No
Secondary Differences in hypersensitivity Symptomfree interval No
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