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The effect of enoxaparin on sudden sensorineural deafness

Phase 2
Recruiting
Conditions
Sudden sensorineural hearing loss.
Sensorineural hearing loss, bilateral
H90.3
Registration Number
IRCT20211010052721N2
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Conscious consent to participate in the study
Patients with sudden sensorineural hearing loss that progresses rapidly and no known cause is found for more than 72 hours

Exclusion Criteria

History of ear diseases
Patients with contraindications to treatment with systemic corticosteroids or anticoagulants such as diabetes mellitus
History of intermittent hearing loss
Pregnancy
Breastfeeding

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Average hearing threshold. Timepoint: Before the intervention and 10 days after starting taking enoxaparin. Method of measurement: Audiometry.
Secondary Outcome Measures
NameTimeMethod
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