Skip to main content
Clinical Trials/JPRN-UMIN000010461
JPRN-UMIN000010461
Completed
未知

Efficacy evaluation of intravitreal aflibercept for polypoidal choroidal vasculopathy - Efficacy evaluation of intravitreal aflibercept for polypoidal choroidal vasculopathy

Yokohama City University Medical Center0 sites30 target enrollmentApril 12, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Yokohama City University Medical Center
Enrollment
30
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 12, 2013
End Date
December 31, 2014
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Lesion size \>\=12 disc area (1 disc rea is 30\.5mm2\). 'Lesion' includes hemorrhage, scar, and CNV. 2\) Area of subretinal hemorrage in study eye\>\=50% of total lesion area 3\) Area of scar or fibrosis in study eye\>\=50% of total lesion area 4\) RPE tear in study eye 5\) Stage 3 or 4 macular hole in study eye 6\) Administration of triamcinolone to study eye within 6 months prior to this study 7\) Administration of dexamethasone to study eye within 30 days prior to this study 8\) Intraocular surgery to study eye within 6 months prior to this study 9\) Any history of vitrectomy in study eye 10\) Any inflammation or infection in intra\-or extra\-ocular tissue in either eye 11\) History of uveitis in either eye 12\) Allergy to fluorescein, indocyanine or iodine 13\) pregnant women and nursing mothers 14\) Patients who were judged by docters to be inappropriate for this study

Outcomes

Primary Outcomes

Not specified

Similar Trials