Study Design: Double-blind clinical trial with 224 patients.
Objective: Evaluate the effectiveness of MFEs in reducing spontaneous symptomatic vitreous opacities (SVOs) and those secondary to vitreous hemorrhage (VH).
Introduction
Vitreous Composition: Comprising collagen fibers and a hydrated extracellular matrix (ECM).
Floaters: Result from vitreous degeneration or blood clots, affecting visual function.
Vitreous Degeneration: Involves HA depolymerization, water loss, and collagen fibril disorganization, leading to floaters.
Study Methods
Participants: 224 patients aged 30-60 years with monocular SVOs.
Trial Groups: Divided into placebo (Vitamin C) and 3 levels of MFE dosage (low, middle, high).
Duration: 3 months, with monitoring of SVOs and visual acuity.
Antioxidant Assay: DDPH test used to compare free radical scavenging ability.