ClinicalTrials.gg
CompletedNCT03313817I-RECANALUpdated Jan 5, 2026

Pre and Post-arterial Recanalization Imaging of Central Retinal Artery Occlusions (CRAO)

An observational study in Retinal Artery Occlusion, Magnetic Resonance Imaging and Diagnosis, sponsored by Fondation Ophtalmologique Adolphe de Rothschild. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-05.

Sponsored by Fondation Ophtalmologique Adolphe de Rothschild · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
63
Ages
18 Years and older
Sex
All
01

Study summary

Central retinal artery occlusions (CRAO) are the equivalent of an ischemic stroke at the retinal level. They share the same risk factors and common pathology. The diagnosis of a CRAO is clinically based on the sudden occurrence of a decrease in deep visual acuity with fundamentally signs of reactive ischemia.

Small studies have highlighted the value of cerebral MRI (Magnetic Resonance Imaging) in CRAO with almost 25% of ischemic strokes found on diffusion sequences and the demonstration of a correlation between anomalies in diffusion sequence and the probability of a pathology with a high risk of recurrence (carotid stenosis or emboligenic cardiopathy). But there are usually few radiological signs that allow a direct positive diagnosis of CRAO, an etiologic diagnosis or a prognosis. This descriptive study will focus on CRAO at the diagnostic and post-treatment phases in the short and medium term, in order to (i) identify imaging etiologic signs of CRAO with specific sequences from a 3 Tesla MRI, (ii) identify positive diagnostic signs of CRAO with the same specific sequences, (iii) correlate these signs with the visual prognosis one month after the CRAO.

02

Conditions studied

  • Retinal Artery Occlusion
  • Magnetic Resonance Imaging
  • Diagnosis
  • Etiology
  • Prognosis
03

In context

Retinal Artery Occlusion

31 studies on the registry are indexed under Retinal Artery Occlusion; 7 are open to participants now.

This study's enrollment of 63 is below the median of 388 across 14 observational studies indexed under Retinal Artery Occlusion.

Browse Retinal Artery Occlusion studies →

Lead sponsor

Fondation Ophtalmologique Adolphe de Rothschild is the lead sponsor of 316 studies on the registry; 78 are open to participants now.

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

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Who can participate

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

Study population

Adult patients hospitalized for CRAO ≤ 48 hours.

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

  • 18 years of age or older
  • CRAO (onset of symptoms ≤ 48 hours)
  • Consent to participate in the study

Exclusion criteria

Exclusion Criteria:

- to 3 Tesla MRI

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
63 participants (actual)
Patient registry
No

Interventions

  • DeviceAdditional MRI sequences

    Patients will be hospitalized for suspicion of CRAO. An "optimized" MRI will be performed with specific sequences: 3D T1 MSDE (Motion Sensitized Driven Equilibrium) "dark blood"; 3D Optimized diffusion centered on the optic nerves; 3D PD T1 after injection. A consultation of ophthalmology and a control MRI will be carried out one month after the CRAO. Again, specific sequences will be added: 3D T1 MSDE (Motion Sensitized Driven Equilibrium) "dark blood"; 3D Optimized diffusion centered on the optic nerves; DTI (Diffusion Tensor Imaging); 3D PD T1 after injection.

06

What researchers measure

Primary outcomes

  1. Contrast enhancement of the ophthalmic artery

    Binary variable (yes/no)

    Time frame: Baseline

  2. Presence of a thrombus

    Binary variable (yes/no)

    Time frame: Baseline

  3. Presence of an arterial stenosis of the supra aortic trunks

    Binary variable (yes/no)

    Time frame: Baseline

  4. Hypersignal of the ophthalmic artery in diffusion

    Binary variable (yes/no)

    Time frame: Baseline

  5. Restriction of the apparent diffusion coefficient (ADC) at the optic nerve level and at the papilla level

    Binary variable (yes/no)

    Time frame: Baseline

07

Study locations

1 site
  • Fondation Ophtalmologique A. de Rothschild
    Paris, 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 Dec 2017 to primary completion in Oct 2023, 70 months.

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

Registered
Sep 25, 2017
First posted
Oct 18, 2017
StartActual
Dec 13, 2017
Primary completionActual
Oct 24, 2023
CompletionActual
Jan 24, 2024
Last update
Jan 5, 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 Jan 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03313817
Responsible party
Sponsor
First posted
Oct 18, 2017
Start date
Dec 13, 2017
Primary completion
Oct 24, 2023
Completion
Jan 24, 2024
Last update
Jan 5, 2026

Oversight

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

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This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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