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Effect of Vitamin Supplementation in Glaucoma Patients

D

Devogelaere Vision

Status

Completed

Conditions

Glaucoma
Abnormal Steady State Pattern Electroretinography
Elevated Retinal Venous Pressure
Homocysteinemia

Treatments

Dietary Supplement: Ocufolin forte

Study type

Observational

Funder types

Other

Identifiers

NCT05080153
151119-OcF

Details and patient eligibility

About

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,

Full 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. .

Enrollment

26 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • glaucoma and/or ocular vascular disease in at least on eye
  • abnormal SSpERG
  • RVP measured using an ophthalmodynamometer at least 15 mmHg higher than intra-ocular pressure (IOP),
  • fasting serum Hcy level > 12 µmol/l
  • stable and well-controlled IOP (with or without IOP-lowering treatment)

Exclusion criteria

  • starting other systemic or ocular medications with potential impacts on RVP within a month before entering the study or during the course of the study
  • starting or changing the dosage of other medications with potential impact on SSpERG within 3 months before entering the study or during the course of the study
  • non-adherence to the follow-up schedule
  • inability to perform a proper RVP measurement using ophthalmodynamometry.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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