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study on effectiveness of methyl prednisolon intratempanic injection in compared to dexametason indoenphatic hydrops and tinnitus cure in definite menier pationts

study on effectiveness of methyl prednisolon intratempanic injection in compared to dexametason indoenphatic hydrops and tinnitus cure in definite menier pationts with using of ECOG test

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015102912691N3
Enrollment
41
Registered
2016-01-19
Start date
2016-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Meniere. Ménière disease

Interventions

Intervention 1: Intrevention group 1: 41 patients with definite Meniere intratympanic methyl prednisolone injections at the clinic undergoing local anesthesia for intratympanic. Intervention 2: Interv
Treatment - Drugs
Intrevention group 1: 41 patients with definite Meniere intratympanic methyl prednisolone injections at the clinic undergoing local anesthesia for intratympanic.
Intervention group 2: 41 patients with definite Meniere intratympanic dexamethasone injections at the clinic undergoing local anesthesia for intratympanic.

Sponsors

Vice Chancellorfor Research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients between 18 and 80 years, did not respond to treatment salt restriction, diuretics and betahistine for three months Exclusion criteria: Disease of neuromuscular system, diseases of the spinal cord and CNS disease of the middle ear, otitis media, conductive hearing loss, taking ototoxic, drug addiction, patients with a history of middle ear surgery, surgical intervention in the inner ear, patients by menier bilateral and perforation of the tympanic membrane and absence of systemic corticosteroid treatment

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Vertigo. Timepoint: Arrival, 2 to 4 weeks, every 6 weeks for 6 to 12 months. Method of measurement: Audiometery Test and questionnaire.

Secondary

MeasureTime frame
Hearing. Timepoint: Arrival, 2 to 4 weeks, every 6 weeks for 6 to 12 months. Method of measurement: Audiometry Test.;Tinnitus. Timepoint: Arrival, 2 to 4 weeks, every 6 weeks for 6 to 12 months. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Elham Masoumi

Tehran University of Medical Sciences

elham.masoumi177@gmail.com+216 6760269

Outcome results

None listed

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