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WithdrawnNCT03435926CORFIUpdated Jun 26, 2026

OCT and Microperimetry in Patients With Active Neovascular ARMD (CORFI)

An observational study in Choroidal Neovascularization, Visual Field, Visual Acuity, sponsored by University Hospital, Limoges. Withdrawn at 1 site in France. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2026-06-26.

Sponsored by University Hospital, Limoges · Observational

Why this study was withdrawn
No inclusion
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
50 Years and older
Sex
All
01

Study summary

ARMD is the main cause of visual disability after 50 years old in France. Patients with active neovascular ARMD are treated with intravitreal injections of antiVEGF. Reinjections criteria are decrease of best corrected visual acuity or active neovascularization's signs (mostly found on macular OCT but also on angiography when necessary).

The aim of this study is to evaluate the link between active neovascularization found on OCT and eye fixation quality measured with microperimetry in ARMD patients treated with antiVEGF.

Quality of eye fixation and exudative signs presents or not present on OCT will be gathered at each consultation over the two-years follow-up for each patient. The mean central retinal sensitivity, the best corrected visual acuity and the bivariate contour ellipse area will also be gathered.

In case no link will be found, for instance bad fixation quality without exudative signs on OCT or good fixation stability despite exudative signs on OCT, microperimetry should have an interest to improve reinjections criteria with a treatment more suitable to the patient.

02

Conditions studied

  • Choroidal Neovascularization, Visual Field, Visual Acuity
03

In context

Choroidal Neovascularization

214 studies on the registry are indexed under Choroidal Neovascularization; 12 are open to participants now.

Browse Choroidal Neovascularization studies →

Lead sponsor

University Hospital, Limoges is the lead sponsor of 264 studies on the registry; 38 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
50 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with active neovascular ARMD treated with antiVEGF

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patients > 50 years old,
  • With neovascular ARMD
  • who need an induction treatment (de novo patients or patients who had their last intravitreal injection of antiVEGF more than 6 months ago)

Exclusion criteria

Exclusion Criteria:

  • Other maculopathies
  • Severe glaucoma with central visual field defect
  • Diabetic patients
  • Corneal, lens or vitreous opacities interfering in OCT analysis
  • Attention or comprehension deficit
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. fixation stability measured by microperimetry and exudative signs on OCT

    quality of eye fixation and exudative signs presents or not present on OCT will be gathered at each consultation over the two-years follow-up. The fixation stability is classified as follows: * Stable if more than 75% of the fixation points are contained inside the circle of 2 degrees of diameter * Relatively unstable if more than 75% of the fixation points are contained within the circle of 4 degrees of diameter and less than 75% contained within that of 2 degrees of diameter * Unstable if less than 75% of the fixation points are contained within the circle of 4 degrees of diameter

    Time frame: 2 years

Secondary outcomes

  1. Bivariate Contour Ellipse Area (BCEA) value

    BCEA will be gathered at each consultation over the two-years follow-up

    Time frame: 2 years

  2. mean central retinal sensitivity

    mean central retinal sensitivity will be gathered at each consultation over the two-years follow-up

    Time frame: 2 years

  3. Best Corrected Visual Acuity (BCVA)

    BCVA will be gathered at each consultation over the two-years follow-up

    Time frame: 2 years

07

Study locations

1 site
  • University Hospital
    Limoges, 87042, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Feb 2018 to primary completion in Jan 2019, 11 months.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 7, 2018
First posted
Feb 19, 2018
StartActual
Feb 13, 2018
Primary completionActual
Jan 22, 2019
CompletionActual
Jan 22, 2019
Last update
Jun 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03435926
Responsible party
Sponsor
First posted
Feb 19, 2018
Start date
Feb 13, 2018
Primary completion
Jan 22, 2019
Completion
Jan 22, 2019
Last update
Jun 26, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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