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Recruiting NCT06910865

Study of the Radio-clinical Correlation of Endolymphatic Hydrops

Observational Endolymphatic Hydrops

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Endolymphatic Hydrops. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

In patients presenting with symptoms of endolymphatic hydrops, signs of vestibular dilation are often found on MRI. Some patients present with these radiological signs without vestibular clinical signs, or signs other than those of hydrops. No study has yet investigated the radiological-clinical correlation of endolymphatic hydrops by selecting patients based on their imaging findings and then comparing them to the symptoms presented.

Primary outcome measures

  • Nystagmus observed on videonystagmoscopy [Time frame: Up to 1 year]

Eligibility criteria

Inclusion criteria

  • Adult subject (≥18 years)
  • Subject presenting vestibular dilation on MRI

Exclusion criteria

  • Subjects who have expressed opposition to the reuse of their data for scientific research purposes.
  • Subjects under legal protection
  • Subjects under guardianship or curatorship

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

France · 1 center
  • Service d'ORL et de Chirurgie Cervico-faciale - CHU de Strasbourg - France — Strasbourg

Identifiers

NCT: NCT06910865 · 9306

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗