The study purpose is to assess the efficacy of VISUPRIMEĀ® eye drops in preventing the conjunctival bacterial load in patients undergoing to anti-VEGF injection.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adult patients (age ā„ 18)
* NaĆÆve and pre-treated patients scheduled for IVI
* Diagnosis of one of the following:
* ARMD
* mCNV
* Proliferative diabetic retinopathy
* Diabetic macular oedema
* Macular oedema secondary to retinal vein occlusion
* The subject has been informed of the nature of the study, agrees to its provisions, and has provided written informed consent, approved by the local Ethics Committee (EC).
Exclusion Criteria:
* Use of systemic antibiotics, corticosteroids within 3 months
* Use of topical antibiotics and or corticosteroids within 15 days from study enrolment
* Use of topical Artificial Tears within 15 days from the enrolment
* Use of topical antiseptic agents within 1 month from study enrolments
* Presence of topical ocular therapies that cannot be suspended for the entire duration of the study
* Ongoing ocular or systemic inflammatory or infectious processes
* Known hypersensitivity to the constituents of the study product
* Diagnosis of Open-Angle Glaucoma
* Uveitis
* Acute and Chronic Conjunctival Disease
* Any intraocular surgery within 6 months from study enrolment, excluded IVI
* Severe and Moderate Dry Eye
* Pregnancy or breast-feeding
* Participation in other clinical studies
* Patients with cognitive impairment and unable to manage home-assigned treatment.