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NCT04499157Terminated

Effect of MEMOPTIC on Visual Field of Patients Followed for a Chronic Open-angle Glaucoma

Source: ClinicalTrials.gov · Last updated 12 Jun 2026

Brief summary (registry, in English)

Open-angle glaucoma is a degeneration of the optic nerve, highlighted by campimetric alterations, and wose only current therapeutic target is the lowering of the intra-ocular pressure (using eye drops, surgery or laser). MEMOPTIC is a tablet combining citicoline, magnesium and Gingko biloba, which have a neuroprotective effect already used in neurodegenerative diseases such as Alzheimer's disease for example. Citicoline has also shown several promising results in ophthalmological diseases (glaucoma, amblyopia or more recently in ischemic optic neuropathies). The citicoline used in eye drops (NEURODROP) has already shown results on the preservation of the vision of glaucomatous patients. The purpose of this project is to determine if MEMOPTIC can have an effect, in addition to the conventional treatments, in the preservation of vision of patients treated for an open-angle glaucoma.

Status (registry)
Terminated
Study type
Interventional
Enrollment
15 (actual)
First submitted
29 Jul 2020
Start date
21 Sept 2020
Primary completion date
18 Jan 2024
Lead sponsor
Centre Hospitalier Universitaire, Amiens
Diseases
Glaucoma
NCT number
NCT04499157

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • diagnosis of cataract or surgery of cataract during the follow-up
  • ocular hypertonia due to a secondary cause (like corticosteroids)
  • general treatment affecting PIO (beta blockers, corticosteroids)

Other illness

  • retinal or macular disease
  • allergy to citicolin
  • history of anterior, intermediate or posterior uveitis

Other

  • pregnancy or breastfeeding

Who the study is looking for

  • diagnosis of GCAO defined by OCT RNFL alterations and visual fields defects
  • age between 20 and 80 years old
  • Well controled intra-ocular pressure under treatment (PIO\<21mmHg or decreased by 20% compared to initial the PIO)

Age in the registry: 20 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
CHU Amiens
Coordinator of this site? Confirm its status
AmiensFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.