Acute Intra Ocular Pressure Monitoring After Aflibercept 8mg/0.07mL

Recruiting N/A Interventional Study
Macular Diseases
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Screening
Participants needed
100 (estimated)
Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · Other
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About This Trial
In just a few years, intravitreal injections have become a standard method of administration for certain retinal deseases (age-related macular degeneration \[AMD\], diabetic edematous maculopathy or retinal vein occlusion \[RVO\]). Thus, vascular endothelial growth factor (anti-VEGF) inhibitors are injected repetitively, every 4 to 6 weeks, in some patients in order to treat such pathologies. It …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient aged 18 or over; * Patient with an indication for Aflibercept 8mg/0.07mL (EYLEA 8mg) * Naive or switched patient, i.e. so-called suboptimal responder to anti-VEGF with high injection frequencies * Patient with rights to social security * Having given free and informed …
Contacts

Magali CESANA

04 83 77 20 60

magali.cesana@ch-toulon.fr

CONTACT