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Research on Precision Diagnosis and Treatment Decision of Common Eye Diseases Based on Artificial Intelligence

Research on Precision Diagnosis and Treatment Decision of Common Eye Diseases Based on Artificial Intelligence

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07078552
Enrollment
368
Registered
2025-07-22
Start date
2024-01-01
Completion date
2025-05-01
Last updated
2025-07-22

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

Conditions

Congenital Ptosis

Keywords

Congenital Ptosis, levator function

Brief summary

The goal of this observational study is to investigate the clinical features of congenital ptosis in children by analyzing eyelid movement captured through smartphone videos. The main question it aims to answer is: Can video-based eyelid measurements and levator muscle function grading provide useful guidance for the treatment of congenital ptosis in children? Participants are children diagnosed with congenital ptosis. Their blinking behavior will be recorded using a smartphone, and eyelid morphology and muscle strength will be assessed from the video data.

Detailed description

In this study, we developed a two-module system for the evaluation of congenital ptosis in children based on smartphone video recordings. The first module performs morphological measurements of eyelid parameters (e.g., palpebral fissure height, margin reflex distance) extracted from blink videos. The accuracy of this module was assessed through agreement analysis between automated measurements and manual measurements performed by clinicians. The second module focuses on levator function grading. The automated grading results were compared against clinical assessments by senior oculoplastic specialists, which served as the gold standard, to evaluate the model's accuracy. Additionally, we compared the model's performance to that of junior ophthalmology residents to assess the system's clinical assistive value in real-world scenarios. Based on these modules, we developed a smartphone-based application for remote ptosis assessment. A multi-center clinical validation study was designed to evaluate the feasibility, consistency, and generalizability of the system in different clinical settings.

Interventions

OTHERptosis

no intervention

Sponsors

Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Tianjin Eye Hospital
CollaboratorOTHER
Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* participants aged ≤18 years with compliance during video recording. Congenital ptosis diagnosis mandated documented symptom onset within the first year of life and bilateral or unilateral MRD1 of \< 2.5 mm

Exclusion criteria

* acquired ptosis, myasthenia gravis, Marcus Gunn syndrome, eyelid deformities, or prior ophthalmic surgery

Design outcomes

Primary

MeasureTime frame
levator function testingOne-time assessment; results available within 1 week of data collection.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026