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Analysis of genotypes associated with the treatment effects of Lucentis for age-related macular degeneratio

Not Applicable
Conditions
age-related macular degeneration
Registration Number
JPRN-UMIN000005584
Lead Sponsor
Kyoto University Graduate School of Medicine, Department of Ophthalmology and Visual Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
600
Inclusion Criteria

Not provided

Exclusion Criteria

Previous treatment with photocoagulation, surgery, photodynamic therapy, Transpupillary thermotherapy, radiation Subfoveal fibrosis or atrophy History of vitrectomy Intraocular surgery within 2 months CNV in either eye due to other causes, such as ocular histo-plasmosis, trauma, or pathological myopia Aphakia or absence of the posterior capsule in the study eye unless it resulted from yttrium aluminum garnet (YAG) posterior capsulotomy in association with prior posterior chamber intraocular lens implantation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
visual acuity change at 12 months after the first treatment
Secondary Outcome Measures
NameTimeMethod
disappearance of retinal exudative change at 3 months, visual acuity change at 3 months, interval for additional treatment, and number of treatment during 12 months
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