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.
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