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Evaluation of The Effect of Nanocurcumin on Treatment of Tinnitus

Phase 3
Recruiting
Conditions
Tinnitus
tinnitus.
H93.1
Registration Number
IRCT20190916044785N1
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
62
Inclusion Criteria

Unilateral or Bilateral Subjective Tinnitus
Age Range: 18-65 Year
Patients do not have Pregnancy and Breastfeeding
Patients do not have Acute or Chronic Ear Infection
Patients do not have Rheumatologic Diseases, Vasculitis, Acoustic Neuroma, Known Neurological Disorders and Ear Surgery
Patients not taking Immunosuppressants such as Interferons, Corticosteroids, Anticonvulsants and Sedatives before starting the study

Exclusion Criteria

Patients who do not willing to enter the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Tinnitus Handicap Inventory. Timepoint: Before and after 21 days of Medicine Consumption. Method of measurement: Tinitus Matching Test.
Secondary Outcome Measures
NameTimeMethod
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