Study on the effects of supplements containing lutein on spontaneous resolution in eyes with chronic central serous chorioretinopathy
Not Applicable
- Conditions
- chronic central serous chorioretinopathy
- Registration Number
- JPRN-UMIN000005372
- Lead Sponsor
- agoya City University Graduate School of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1. presence of hard exudate or subretinal hemorrhage in or around serous retinal detachment 2. past history of photocoagulation or photodynamic therapy 3. presence of other macular diseases 4. presence of uveitis 5. myopia with -8D or higher 6. past history of vitrectomy 7. hazy media causing difficulties in fundus examinations 8. active exudative age-related macular degeneration in a fellow eye 9. allergic to lutein, anti-oxidants, and minerals 10. daily take of lutein, anti-oxidants, or other supplements 11. pregnant or planned for pregnancy 12. undergone intraocular surgeries within the previous 6 months 13. judged by the investigator to be ineligible for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method (1) Rate of spontaneous resolution of central serous chorioretinopathy (2) Changes in macular volume measured by optical coherence tomography
- Secondary Outcome Measures
Name Time Method Best-corrected visual acuity