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Evaluation of different materials for aural fullness treatment and the effect of local anesthetics as its diagnostic tool

Evaluation of different materials for aural fullness treatment and the effect of local anesthetics as its diagnostic tool - Aural fullness treatment with a tympanic membrane patch and its diagnosis with local anesthetics.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021233
Enrollment
100
Registered
2018-04-01
Start date
2014-02-01
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

Disorders presenting aural fullness

Interventions

The local anesthetics of the tympanic membrane Tympanic membrane patch

Sponsors

Department of Otolaryngology, Nagoya City University, Graduate School of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Complaining aural fullness or similar symptoms 2) 16 years or older when registering 3) Capable to submit a written consent form 4) Capable to be present at ENT clinic of Nagoya City University Hospital.

Exclusion criteria

Exclusion criteria: 1) Tympanic membrane with perforation 2) Presenting sensory symptoms due to systemic neurological, psychological or collagen diseases 3) Severe infectious disease 4) Medications with potential complications for the sensory systems 5) Diabetes that is poorly controlled 6) Hepatic disease (AST >100U and/or ALT 100U) 7) Renal malfunction (BUN>25mg/ml and/or serum Cre level> 2.0,g/dl) 8) Impaired wound healing 9) Pregnant, or potentially pregnant woman 10) Participating other clinical trials within three months prior to the trial 11) Allergy to the amide type local anesthetics and metals 12) Taking loop diuretics, thiazide, isosorbide or other drugs separately specified. 13) Presenting acute/chronic otitis media, external otitis, tympanic membrane inflammation and aural diseases separately specified. 14) Heart pacer implantation 15) Carrying other medical issues the investigator considered not suitable for the trial

Design outcomes

Primary

MeasureTime frame
Correlation of the extent of relieving by the local anesthetics and diagnostic criteria of the patients

Secondary

MeasureTime frame
Correlation of the extent of relieving by the tympanic membrane patch and diagnostic criteria of the patients

Countries

Japan

Contacts

Public ContactAkira Inagaki

Nagoya City University Hospital Department of Otolaryngology

meijo_ent@hotmail.com052-853-8256

Outcome results

None listed

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