AOSLO-Based Precise Measurement of Retinal Hemodynamics: Development and Application Assessment

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-30
SponsorZhongshan Ophthalmic Center, Sun Yat-sen University

About this trial

Changes in retinal hemodynamics play a key role in the development of various eye diseases. Currently, mainstream hemodynamic evaluation techniques have low resolution and poor measurement accuracy, limiting their widespread application. Adaptive optical laser scanning ophthalmoscopy (AO-SLO) can capture retinal vascular images at the cellular level, offering the potential for high-precision retinal hemodynamic evaluation. This project will: ① innovate the AO-SLO blood flow imaging scanning module and acquisition mode, develop algorithms for extracting spatiotemporal signal features from blood flow images, and achieve quantitative analysis of retinal hemodynamics based on AO-SLO; ② construct an in vitro retinal hemodynamic measurement simulation eye, conduct multidimensional AO-SLO hemodynamic measurements, and establish an intelligent model for precise calibration of retinal hemodynamic parameters; ③ conduct AO-SLO-based retinal hemodynamic studies in high myopia, integrating multi-modal ophthalmic imaging to investigate the patterns of changes in retinal vascular structure and blood flow function in high myopia. Ultimately, a new precision measurement imaging technology platform for retinal hemodynamics will be established.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants must understand the clinical study and voluntarily participate, and sign an informed consent form;

Age 18-30 years old, no gender restrictions;

Equivalent spherical power≤0D cylindrical power -2.0D to +2.0D, best-corrected visual acuity ≥ 1.0

Disqualifiers

Participants with significant refractive media opacity-related conditions (severe cataracts, vitreous diseases, corneal diseases, etc.) at screening, or unable to complete or cooperate with routine ophthalmic examinations;

History of or concurrent conditions such as ptosis, nystagmus, diabetic retinopathy, various macular degeneration, retinal vascular diseases, optic nerve inflammatory diseases, primary angle-closure glaucoma, various secondary glaucoma, amblyopia, or severe strabismus

History of previous eye surgery

Patients with severe hypertension, diabetes, or other systemic diseases that cause secondary changes in the retina

Trial population

The people From Guangzhou, Guangdong Province, China

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 2 trial groups
Group A: myopia, low and middle grade
Group B: myopia, high grade

Trial outcomes

Primary outcomes

1

Blood flow velocity in the central arteries and veins of the retina

Measure the blood flow velocity and flow velocity standard deviation of the central arteries and veins of the retina of the subject using an adaptive optical laser scanning ophthalmoscope.

Time frame
7 days after the enrollment
2

The structure of central retinal arteries and veins

Measure the diameter of the central arteries and veins of the retina, the thickness of the vessel walls, and the wall-to-lumen ratio of the subjects using an adaptive optics laser scanning ophthalmoscope.

Time frame
7 days after the enrollment
3

Retinal and choroidal capillary morphological parameters

Use OCTA to obtain images of superficial and deep capillaries and choroidal capillaries within a 3×3 mm area of the posterior pole of the retina, and use a proprietary algorithm to extract morphological parameters.

Time frame
7 days after the enrollment

Secondary outcomes

1

The examination for anterior segment of eyes

Use a slit lamp microscope to examine the cornea, conjunctiva, anterior chamber, lens, and other anterior structures of the anterior segment of the eye

Time frame
Baseline
2

Axis of the eye

Measure the axial length of the subject's eye using the IOL-Master 500

Time frame
Baseline
3

Best corrected vision cutiy

Assess the best corrected vision by subjective refraction

Time frame
Baseline
4

Intraocular pressure

Measure intraocular pressure in both eyes using a non-contact tonometer.

Time frame
Baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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