NCT07796633

Brief Summary

VHIT Sometimes demonstrate preserved semicircular canal function with corrective ,normal VOR gain or mild abnormalities

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P25-P50 for all trials

Timeline
6mo left

Started Aug 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress26%
Aug 2026Apr 2027

Study Start

First participant enrolled

August 1, 2026

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

August 23, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 1, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2027

Last Updated

September 1, 2026

Status Verified

August 1, 2026

Enrollment Period

7 months

First QC Date

August 23, 2026

Last Update Submit

August 30, 2026

Conditions

Definite Vestibular MigraineMigraine

Outcome Measures

Primary Outcomes (1)

  • Change in vestibulo-ocular reflex (VOR) gain of the six semicircular canals (right and left horizontal, anterior, and posterior canals) in 30 normal patients and 30 patients with vestibular migraine measured by video Head Impulse Test (vHIT).

    Change in vestibulo-ocular reflex (VOR) gain of the six semicircular canals (right and left horizontal, anterior, and posterior canals) in 30 normal patients and 30 patients with vestibular migraine measured by video Head Impulse Test (vHIT).

    6 months

Study Arms (2)

cases of definite Vestibular migrane

Other: No Intervention: Observational Cohort

control :normal patients

Other: No Intervention: Observational Cohort

Interventions

No Intervention: Observational CohortOTHER

No intervention

cases of definite Vestibular migranecontrol :normal patients

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

case control

You may qualify if:

  • diagnosis of definite Vestibular migraine.
  • Ability to cooperate with vestibular testing
  • consent to participate

You may not qualify if:

  • Benign proximal positional vertigo
  • Menier's disease
  • vestibular neuritis
  • chronic otitis media
  • previous surgery in ears
  • Sensironeral hearing loss unrelated to migraine
  • neurological disease affecting balance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Migraine Disorders

Condition Hierarchy (Ancestors)

Headache Disorders, PrimaryHeadache DisordersBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident at audiovestibular medicine ENT department Sohag university

Study Record Dates

First Submitted

August 23, 2026

First Posted

September 1, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

April 1, 2027

Last Updated

September 1, 2026

Record last verified: 2026-08