AMD Clinical Trial
Official title:
Real World Study to Evaluate the Improving Effects of Visucomplex Plus on Quality of Life in Patients With Dry and Wet Age-related Macular Degeneration (AMD)
This is an observational study in which patients affected by dry or wet AMD will be enrolled,
after signing the Informed Consent, according to eligibility criteria.
Patients, after signing the Informed Consent, will enter into a screening phase during which
the concomitant medication, clinical history, physical examination (including smoking habits)
will be checked and the inclusion/exclusion criteria will be assessed.
Then, at the time of Baseline visit (V0) the eligible patients will be given Visucomplex Plus
as monotherapy, 1 capsule daily after food, or for dry or wet AMD patients under treatment
with a stable dose of an anti-VEGF drug, Visucomplex Plus, 1 capsule daily after food, upon
physical decision.
Screening phase and the baseline visit (V0) could coincide.
n/a
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