Finasteride effect as a treatment for spontaneous retinal edema
Phase 1
- Conditions
- Central Serous Chorioretinopathy.Separation of retinal layers
- Registration Number
- IRCT2013083114530N1
- Lead Sponsor
- Shahid Sadoughi University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Eligibility criteria:patients with chronic CSCR, which was defined in this study as 1) the presence of subretinal fluid, as determined by spectraldomain OCT;2)the subretinal fluid must have been present for at least 3 months or there was a recurrence of subretinal fluid in ipsilateral eye within the past 3 months.
exclusion criteria:corticosteroid use,CNV or other ocular disease that disturb the study outcome,pregnant and nursery women
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Best corrected visual acuity. Timepoint: by the intervention initiation,15 days,1,2 and 3 months after intervention,3months after discontinuation of intervention. Method of measurement: Snellen chart.;Central macular thickness. Timepoint: by the intervention initiation,15 days,1,2 and 3 months after intervention,3months after discontinuation of intervention. Method of measurement: spectral domain OCT.;Subretinal fluid volume. Timepoint: by the intervention initiation,15 days,1,2 and 3 months after intervention,3months after discontinuation of intervention. Method of measurement: spectral domain OCT.
- Secondary Outcome Measures
Name Time Method Adverse effects(decreased libido,impotence,improper ejaculation,postural hypotension,dizziness). Timepoint: 15 days,1,2 and 3 months after intervention. Method of measurement: pation history taking.