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Assessment of Visual Acuity in Patients With Polypoidal Choroidal Vasculopathy and Aflibercept Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02381730
Acronym
PCV
Enrollment
37
Registered
2015-03-06
Start date
2014-01-31
Completion date
2017-08-31
Last updated
2017-12-08

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

Conditions

Polypoidal Choroidal Vasculopathy

Brief summary

Polypoidal choroidal vasculopathy (PCV) is a disease of the choroidal vasculature, that is often regarded as a sub-type of age-related macular degeneration (AMD). However, PCV response to anti-vascular agents differs from the response of typical AMD. This study aims at describing the evolution of the best corrected visual acuity (BCVA) in PCV patients, 28 weeks after they receive one injection of intravitreal aflibercept (2mg).

Interventions

Patient receive one intravitreal injection of 2mg aflibercept (as currently recommended in the treatment of AMD)

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Active polypoidal choroidal vasculopathy, * Visual acuity superior to 1/10 (20/200) and inferior to 6,25/10 (20/32) * Age above 45 * No prior intravitreal treatment, or no response to prior treatment by 3 injections of ranibizumab, or disease recurrence after more than 3 months of stability * Intravitreal injection of aflibercept is indicated by current clinical recommendations

Exclusion criteria

* Simultaneous treatment with another anti-VEGM agent * Diabetic retinopathy * Personal history of vitrectomy or uveitis * Personal history laser photocoagulation and/or verteporphin phototherapy * Tear in the pigmentary epithelium * Chorioretinitis scar * Macular atrophy in the pigmentary epithelium * Treatment with corticosteroids * Eye surgery less than 3 months before inclusion

Design outcomes

Primary

MeasureTime frame
Evolution of the best corrected visual acuity (BCVA) measured on the EDTRS scale, between pre-injection and 28 weeks after injection28 weeks

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026