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A multicenter cohort study of clinical features, treatment, and outcome of bilateral vestibulopathy and presbyvestibulopathy

A multicenter cohort study of clinical features, treatment, and outcome of bilateral vestibulopathy and presbyvestibulopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108314
Enrollment
Unknown
Registered
2025-08-28
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bilateral vestibulopathy and Presbyvestibulopathy

Interventions

Group of bilateral vestibulopathy or presbyvestibulopathy:Not applicable

Sponsors

Eye and ENT Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Participants voluntarily agree to participate in the study and sign the informed consent form; 2.Aged between 18 and 85 years; 3.Diagnosed with or clinically suspected of having bilateral vestibulopathy or presbyvestibulopathy.

Exclusion criteria

Exclusion criteria: 1. Patients with balance dysfunction combined with other causes (including cerebellar lesions, vestibular neuritis, multiple sclerosis, etc.); 2. Patients complicated with serious systemic diseases or mental disorders and unable to complete follow-up; 3. The investigator thinks that there are other reasons for not participating in this clinical study.

Design outcomes

Primary

MeasureTime frame
Balance Function;—

Secondary

MeasureTime frame
Vestibular function;Threshold of pure tone hearing;—

Countries

China

Contacts

Public ContactLi Weihua;Wang Wuqing

Eye and ENT Hospital of Fudan University

wwuqing@eent.shmu.edu.cn+86 138 1688 0591

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026