Skip to content

Search for inner ear window permeability using 17O-MRI

Search for Inner Ear Window Permeability Using 17O-MRI Method

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs041210085
Enrollment
35
Registered
2021-10-18
Start date
2021-11-16
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy adult, Meniere's disease Meniere's disease, endolymphatic hydrops

Interventions

Intratympanic administration of PSO17

Sponsors

Sone Michihiko
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: STEP 1: (1) Healthy adults 20 years and older (2) Persons who have received sufficient explanation of the contents of this research and have obtained their written consent. (3) Those who are 20 years of age or older when obtaining consent. STEP2: (1) Definite and probable cases of Meniere's disease as defined in the diagnostic criteria for Meniere's disease 2017 of the Japanese Society for Equilibrium research. (2) Patients who have received sufficient explanation of the contents of this study and have given their written consent. (3) The subject must be 20 years of age or older when obtaining consent.

Exclusion criteria

Exclusion criteria: Persons who fall under any of the following shall be excluded. (1) Patients with implanted or implanted medical devices, etc., containing metal (except for medical devices that have been conditionally approved for compatibility with MRI systems), patients with tattoos on the upper body, or patients who cannot undergo MRI examinations due to claustrophobia, etc. (2) Patients with severe scoliosis (3) Patients suffering from other mental disorders (4) Patients who are pregnant or suspected to be pregnant, those who plan or refuse to deny pregnancy, including their partners during the study period, and lactating patients (5) Patients who are deemed unsuitable for participation in the study by the principal investigator or sub-investigator and have difficulty with MRI study.

Design outcomes

Primary

MeasureTime frame
Evaluate if O17 migration to the perilymph and endolymphatic hydrops can be depicted

Secondary

MeasureTime frame
safety

Contacts

Public ContactTadao Yoshida

Nagoya university hospital

tadaoy@med.nagoya-u.ac.jp+81-52-744-2323

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026