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Treatment with aflibercept for AMD cases with better value in optometry

Treatment with aflibercept for AMD cases with better value in optometry - Treatment with aflibercept for AMD cases with better value in optometry (TAABO study)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012221
Enrollment
30
Registered
2013-11-06
Start date
2013-11-07
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

age-related macular degeneration

Interventions

treatment with Eylea

Sponsors

Keio University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Willingness to provide written informed consent 2)AMD with Subfoveal lesion on fluorescent angiography, indocyanine green angiography and/or optical coherence tomography 3)AMD eyes which had not been treated with PDT and/or anti-VEGF 4)baseline BCVA in the study eye over 0.5

Exclusion criteria

Exclusion criteria: 1)Prior treatment with triamcinolone (<3 montsh 2)Prior treatment with dexamethasone <30 days) 3)Prior intraocular surgery (<3 months) 4)Prior vitrectomy 5)Hypersensitivity or allergy to fluorescein or indocyanine green, clinically significant drug allergy or known hypersensitivity to therapeutic or diagnostic protein products 6)Patient with pregnancy or its possibility, and with breast-feeding 7)Patient who the doctor in charge judges are ineligible for the study

Design outcomes

Primary

MeasureTime frame
Percentage of patients with less exudative changes on optical coherence tomography(OCT) at month 6

Secondary

MeasureTime frame
Results of visual acuity, OCT, angiography, and QOL research

Countries

Japan

Contacts

Public ContactYoko Ozawa

Keio University, School of Medicine Department of Ophthalmology

ozawa@a5.keio.jp03-3353-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026