Evaluation of the effect of topical aminophylline in hyposmic and anosmic patients
Phase 3
Recruiting
- Conditions
- R43.0Patient with Post viral hyposmia.Anosmia
- Registration Number
- IRCT20220104053625N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
patients older than 18 years
diagnosis of post viral hyposmia or anosmia, the course of olfactory dysfunction was > 6 months
signing the written informed consent to participate study
Exclusion Criteria
lack of proper compliance to the prescribed drugs
history of nasal or skull base surgeries, history of nasal polyps, history of facial or nasal trauma
allergies to aminophylline or theophylline
consumption of other drugs.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patients' olfactory level. Timepoint: Before the intervention and three months after taking the drops. Method of measurement: SIT (smell identification test).
- Secondary Outcome Measures
Name Time Method