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Application of adaptive optics fundus imaging system combined with multimodal imaging technology in retinal diseases

Application of adaptive optics fundus imaging system combined with multimodal imaging technology in retinal diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113550
Enrollment
Unknown
Registered
2025-12-01
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Patients with fundus diseases (including early-stage diabetic retinopathy, early-stage age-related macular degeneration, central serous chorioretinopathy, and inherited retinal diseases)

Interventions

Early diabetic retinopathy group:None
Normal control group:None
Early age-related macular degeneration group:None
Contral serous chorioretinopathy group:None

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with the following retinal diseases are eligible: including, but not limited to, retinal vascular diseases (e.g., diabetic retinopathy, retinal vein occlusion), macular diseases (e.g., dry age-related macular degeneration, central serous chorioretinopathy), inherited retinal disorders (e.g., retinitis pigmentosa, cone-rod dystrophy, occult macular dystrophy), and other fundus conditions. There are no restrictions regarding age or sex. Specifically, for diabetic retinopathy (DR), the study will primarily enroll patients with early-stage DR. This is defined according to the International Clinical Diabetic Retinopathy Disease Severity Scale as DR Stage I patients, i.e., those with early non-proliferative diabetic retinopathy (NPDR) presenting only with microaneurysms. 2.There are no restrictions regarding age or sex; 3.Patients voluntarily participate in the study and provide informed consent; 4.Good study compliance; 5.If both eyes meet the image quality standards, then both are included in the analysis. If only one eye meets the standards, then that eye alone is included.

Exclusion criteria

Exclusion criteria: 1.Subjects with an intraocular pressure (IOP) greater than 21 mmHg in either eye, or with any other condition that contraindicates pupillary dilation; 2.Aphakia; 3.Subjects with opacities of the refractive media that preclude the acquisition of satisfactory images; 4.Subjects with poor fixation or any other condition that precludes adequate cooperation during the examination; 5.Vulnerable populations, such as pregnant women, minors, and individuals with psychiatric disorders; 6.Deemed unsuitable for participation in the clinical study by the investigator.

Design outcomes

Primary

MeasureTime frame
Cone Photoreceptors: cell density, cell spacing, spacing standard deviation, cell regularity Vascular Blood Flow: retinal vessel wall thickness, vascular lumen diameter, vascular diameter;Fundus autofluorescence;Central macular thickness;Vessel blood flow: retinal vessel wall thickness, lumen diameter, vessel diameter, wall-to-lumen ratio, blood flow velocity;

Countries

China

Contacts

Public ContactSun Zuhua

Eye Hospital, Wenzhou Medical University

susan0402@163.com+86 577 88075582

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026