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Boarding Ring Glasses Versus Placebo Glasses or Not Glasses in the Treatment of Vestibular Neuritis (NEVRING)

R

Regional University Hospital Center (CHRU)

Status

Enrolling

Conditions

Vestibular Neuritis

Treatments

Diagnostic Test: Caloric test
Diagnostic Test: Angle of deviation at Fukuda
Other: EHTEV questionnaire
Other: EEV questionnaire
Diagnostic Test: Alexander's degree of nystagmus
Diagnostic Test: Measurement of the speed of Nystagmus
Other: anxiety VAS

Study type

Interventional

Funder types

Other

Identifiers

NCT04678167
29BRC20.0040

Details and patient eligibility

About

Vestibular neuritis is a brutal and continuous dizzying syndrome of peripheral (vestibular) origin without cochlear or other associated involvement. Specifically, vestibular neuritis is inflammation of the nerve that innervates the vestibular canals (the inner ear). It is characterized by the sudden onset of intense and prolonged vertigo accompanied by postural imbalance, nausea and vomiting, without hearing impairment or other neurological symptoms. Vestibular neuritis is the second cause of peripheral vertigo after benign paroxysmal positional vertigo. It represents approximately 7% of patients consulting for vertigo. The purpose of this study is to evaluate if wearing Boarding Ring glasses can be accelerated vestibular compensation.

Enrollment

51 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adult patients,
  • patient with vestibular neuritis defined by appearance of continuous rotating vertigo with nausea
  • patient with spontaneous horizonto-rotating nystagmus beating towards the healthy ear
  • patient with a postural deviation towards the affected ear;
  • vestibular hyporeflexia measured at the caloric tests greater than 25%
  • patient who has given free, enlighten and written consent

Exclusion criteria

  • patient with a history of vertigo of vestibular origin or with vertigo developing for more than 4 days
  • patient with associated hearing loss or tinnitus
  • patient with an motor ocular abnormality of central origin
  • patient refusal or inability to consent

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

51 participants in 3 patient groups, including a placebo group

Boarding ring glasses
Experimental group
Description:
Realization of the following examinations WITH Boarding ring glasses : * caloric tests, * measurement of the speed of Nystagmus, * angle of deviation in Fukuda, * Alexander's degree of nystagmus, * EHTEV and EEV questionnaires, * anxiety VAS
Treatment:
Other: EHTEV questionnaire
Diagnostic Test: Angle of deviation at Fukuda
Diagnostic Test: Alexander's degree of nystagmus
Other: anxiety VAS
Diagnostic Test: Measurement of the speed of Nystagmus
Other: EEV questionnaire
Diagnostic Test: Caloric test
Placebo glasses
Placebo Comparator group
Description:
Realization of the following examinations WITH Placebo glasses : * caloric tests, * measurement of the speed of Nystagmus, * angle of deviation in Fukuda, * Alexander's degree of nystagmus, * EHTEV and EEV questionnaires, * anxiety VAS
Treatment:
Other: EHTEV questionnaire
Diagnostic Test: Angle of deviation at Fukuda
Diagnostic Test: Alexander's degree of nystagmus
Other: anxiety VAS
Diagnostic Test: Measurement of the speed of Nystagmus
Other: EEV questionnaire
Diagnostic Test: Caloric test
No glasses
Other group
Description:
Realization of the following examinations WITHOUT glasses : * caloric tests, * measurement of the speed of Nystagmus, * angle of deviation in Fukuda, * Alexander's degree of nystagmus, * EHTEV and EEV questionnaires, * anxiety VAS
Treatment:
Other: EHTEV questionnaire
Diagnostic Test: Angle of deviation at Fukuda
Diagnostic Test: Alexander's degree of nystagmus
Other: anxiety VAS
Diagnostic Test: Measurement of the speed of Nystagmus
Other: EEV questionnaire
Diagnostic Test: Caloric test

Trial contacts and locations

3

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Central trial contact

Jean-Christophe LECLERE, Dr

Data sourced from clinicaltrials.gov

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