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Arterial Spin Labeling MRI for Assessing Blood Perfusion in the Human Eye Repeatability Study and Clinical Application

Arterial Spin Labeling MRI for Assessing Blood Perfusion in the Human Eye Repeatability Study and Clinical Application

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05724641
Acronym
PerfRet
Enrollment
70
Registered
2023-02-13
Start date
2023-01-10
Completion date
2026-06-30
Last updated
2025-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinal Diseases

Brief summary

The MRI perfusion imaging using arterial spin labeling (ASL)'s non-invasive technique (i.e. without injection of contrast medium) allows, thanks to recent technological improvement of the spatial resolution, measuring several perfusion parameter of the retinal tissue such as the regional Blood Flow (rBF) or the cerebral blood flow (cBF) expressed in ml/100g/min. Reliable application of ASL thus requires the precision and specificity of the MRI protocol to be tested.

Interventions

DIAGNOSTIC_TESTMRI perfusion imaging using ASL's non-invasive technique

Patients will undergo through an MRI-scan using the ASL MRI sequence, as described per protocol.

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Carrier of target pathologies: TAO optic neuropathy, inflammatory optic neuropathy, ischemic optic neuropathy. * no cardiovascular risk factors or other ophthalmological pathology * adhere to the study protocol after reading the patient information document * signe the informed consent form to participate in the study * do not have any contraindications to an MRI examination

Exclusion criteria

* Usual contraindications to MRI (Pacemaker, Metallic foreign body, Cochlear implant,…) * Severe claustrophobia

Design outcomes

Primary

MeasureTime frameDescription
Repeatability measurement on volunteers2 monthimplementing a protocol based on 2 imaging sessions : 1st session with 2 ASL sequences and a 2nd session scheduled 5-7 days later in similar conditions including 1 ASL in volunteers will be applied. This protocol allows assessing the intra-day and the inter-day variability of the measurements using Intra-Class Correlation Coefficient and metric derived from Bland-Altman plots. A total of 20 MRI examinations are planned for this phase of the study.

Secondary

MeasureTime frameDescription
Mesurement of the retinal perfusion by MRI ASL in patient in acute phase4 yearsAnalysing the retinal perfusion by ASL to be able to figure out if the decreased visual acuity has an ischemic etiology.
Mesurement of the retinal perfusion by MRI ASLin patient in a chronic phase4 yearsFollowing up the disease process (stability, progression or reversal of the decrease in visual acuity).

Countries

Belgium

Contacts

Primary ContactIdil Günes-Tatar, MD
idil.gunes@saintluc.uclouvain.be+32.276442544
Backup ContactThierry Duprez, MD
thierry.duprez@saintluc.uclouvain.be+32.276442919

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026