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The effect of rivaroxaban on hearing loss

Comparison and evaluation of the effect of rivaroxaban in the complementary treatment of sudden sensorineural hearing loss

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110603006699N5
Enrollment
34
Registered
2021-03-09
Start date
2021-03-10
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Decreased sensorineural hearing. Unspecified sensorineural hearing loss

Interventions

Intervention 1: Intervention group: Rivaroxaban 10 mg tablets of the ?Arena company are received daily for 10 days. Intervention 2: Control group: Placebo tablets with the same shape and color are ta

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of SNHL by an ENT specialist Reduction of more than 30 dB in hearing at least 3 frequencies Body mass index between 18-30 kg per square meter Negative pregnancy test in women of reproductive age 15-35 years Normal coagulation tests Normal renal function Regular visits for follow up Consent to enter the study

Exclusion criteria

Exclusion criteria: Previous hemorrhagic diseases such as intracranial hemorrhage Previous coagulation diseases History of previous thrombosis anywhere on the body Active stomach ulcers History of psychiatric diseases Any previous illness or surgery on the ears Any signs of inflammation or infection of the ear on examination History of hearing loss Meniere's disease Recent vocal or compressive trauma Underlying disease that may be the cause of SNHL, such as trauma, autotoxic drugs, infection, etc Blood pressure higher than 180/110 Uncontrolled diabetes Hypersensitivity reaction to corticosteroids Taking drugs such as methadone

Design outcomes

Primary

MeasureTime frame
Pure tone audiometry Level. Timepoint: Beginning and end of the study. Method of measurement: Audiometric device.;Word recognition score level. Timepoint: Beginning and end of the study. Method of measurement: Audiometric device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan moshtaghi

Esfahan University of Medical Sciences

ehsan_moshtaghi1989@yahoo.com0098312330066

Outcome results

None listed

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