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the SDMEAI Study: a Multi-center Epidemiological Study

Effects of Systemic Diseases and Medications on Eye and Artificial Intelligence Model Development: a Multi-center Epidemiological Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04849819
Enrollment
1000
Registered
2021-04-19
Start date
2021-04-22
Completion date
2026-04-22
Last updated
2021-04-20

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

Conditions

Adverse Drug Effect on Eye, Artificial Intelligence, Eye Involvement of Systemic Diseaes

Brief summary

A variety of diseases in the Department of Rheumatology, Immunology, Nephrology, and Gastroenterology can cause eye lesions, and medications can also bring various adverse reactions, which can seriously reduce the quality of patients' daily life, bring additional economic burdens, and even threaten the lives of patients. This study aims to recruit patients from the aboved-mentioned departments and conduct a cross-sectional and cohort study. On one hand, we plan to compare the epidemiological characteristics of ocular lesions of systemic diseases and eye adverse drug effects in patients with rheumatology, immunology, nephrology and gastroenterology, and summarized some epidemiological indices such as prevalence, high-risk factors, etc. On the other hand, we plan to develop an artificial intelligence model after collecting certain case data. By selecting risk factors related to the occurrence of ocular lesions, we aim to train models that can predict the ocular manifestations of systemic diseases and medications.

Interventions

DRUGCorticosteroids, immunosuppressors, biological agents

We do not prescribe new medications to patients but only observe their adverse effects on the eye.

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 6-80 years old, gender is not limited * patients who have been diagnosed with systemic diseases; * patients who have ever or never used any ocular toxic drugs such as corticosteroids, chloroquine, etc.; * no history of glaucoma, cataract, scleritis, uveitis, ocular trauma, etc. before enrollment; * willing to complete follow-ups for at least 2 years.

Exclusion criteria

* Mainly use local therapies (intraocular, intra-articular and other non-systemic drug routes); * history of intraocular surgery (such as lens implantation, vitrectomy, retinal photocoagulation); * history of glaucoma, cataract, center serous retinopathy, etc.; * history of various diseases (such as scleritis, uveitis, eye trauma, etc.) that may cause opacity of the eye under the posterior capsule; * any other diseases or conditions that affect the observation, such as diabetes, low calcium convulsions, long-term exposure to radiation before enrollment; * subjects with endogenous corticosteroids, or psychiatric diseases.

Design outcomes

Primary

MeasureTime frameDescription
morbidity2021.4.22-2025.4.22Morbiditys of various ocular lesions.

Contacts

Primary ContactHaotian Lin, Ph.D.
haot.lin@hotmail.com13802793086

Outcome results

None listed

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