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Clinical Trial Summary

The impact of targeted vitamin supplementation on retinal venous pressure (RVP) and steady state pattern ERG (SSpERG) in patients with RVP 15mmHg or more above intra-ocular pressure (IOP) and serum homocystein 12µmol/l or more, with signs of progression in spite of adequate IOP control, as evidenced by SSpERG abnormality with or without structural progression or visual field progression,


Clinical Trial Description

Provided the inclusion criteria were met, RVP measurement was repeated, and a 1 capsule/day regimen of Ocufolin® forte was subsequently carried out for a duration of 3 months, after which repeat measurements of IOP, SSpERG, and RVP were performed, along with dilated fundoscopy. . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05080153
Study type Observational
Source Devogelaere Vision
Contact
Status Completed
Phase
Start date November 15, 2019
Completion date June 30, 2021

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