Evaluation of The Effect of Nanocurcumin on Treatment of Tinnitus
Phase 3
Recruiting
- Conditions
- Tinnitustinnitus.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
Name Time Method Tinnitus Handicap Inventory. Timepoint: Before and after 21 days of Medicine Consumption. Method of measurement: Tinitus Matching Test.
- Secondary Outcome Measures
Name Time Method