Clinical Trials Directory

Trials / Completed

CompletedNCT05527106

Evaluation of the Effect of Citicoline and Docosahexaenoic Acid (DHA) on the Visual Function of Patients With Glaucoma

Evaluation of the Effect of Citicoline (Cebrolux 800 mg) and Docosahexaenoic Acid (DHA) Compound (BrudyPio 1.5 g) on the Visual Function of Patients With Glaucoma With a Pilot Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
73 (actual)
Sponsor
Institut Catala de Retina · Academic / Other
Sex
All
Age
50 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Pilot, single-blind, randomized and controlled study to evaluate the changes produced in the visual function of patients with glaucoma after oral administration for 3 months of citicoline and docosahexaenoic Acid (DHA) vs citicoline and docosahexaenoic Acid (DHA) vs vitamin C.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCiticolineEvery subject randomized into this group have to take 2 sachets of Cebrolux 800 (362 mg of citicoline per day), every day, for 3 months.
DIETARY_SUPPLEMENTDocosahexaenoic Acid (DHA)Every subject randomized into this group have to take 3 pills of Brudypio 1.5g (1050 mg of DHA per day), every day, for 3 months.
DIETARY_SUPPLEMENTCiticoline and Docosahexaenoic Acid (DHA)Every subject randomized into this group have to take 2 sachets of Cebrolux 800 and 3 pills of Brudypio 1.5g per day, every day, for 3 months.
DIETARY_SUPPLEMENTVitamin CEvery subject randomized into this group have to take 1 pills of Vitamin C (500 mg per day), every day, for 3 months.

Timeline

Start date
2015-03-12
Primary completion
2022-05-25
Completion
2022-05-25
First posted
2022-09-02
Last updated
2022-09-02

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05527106. Inclusion in this directory is not an endorsement.