Skip to content

Xinxing Eye Cohort Study

Xinxing Eye Cohort Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07257536
Enrollment
3000
Registered
2025-12-02
Start date
2025-12-15
Completion date
2028-11-30
Last updated
2025-12-02

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

Conditions

Cataract, Refractive Errors

Brief summary

To establish the baseline levels and monitor the progress of two newly introduced global eye health indicators in Xinxing County, including effective refractive error coverage (eREC) and effective cataract surgery coverage (eCSC). And to assess the prevalence and treatment status of common eye disease in Xinxing County.

Interventions

None listed

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Primary and secondary school students in Xinxing County and people covered by the national basic public health service, including children aged 0-6, seniors over 65 years old and diabetic patients, etc. * Voluntarily participate in this study and provide signed informed consent

Exclusion criteria

* Unable to cooperate with research-related examinations, such as those with disabilities, communication barriers, or other reasons that prevent examinations * With serious systemic disease that may affect the examination, or participating in the research examination may endanger one's health * Other people who the researchers consider unsuitable to participate in this study

Design outcomes

Primary

MeasureTime frameDescription
Visual acuitythrough study completion, an average of 1 yearTest and record uncorrected visual acuity; if the participant wears glasses, measure the best corrected visual acuity with glasses. For participants with poor unaided or corrected visual acuity (\<4.7), perform additional pinhole visual acuity testing.

Secondary

MeasureTime frameDescription
Strabismusthrough study completion, an average of 1 yearAssess strabismus status and angle at both near and distance fixation.
Autorefractionthrough study completion, an average of 1 yearMeasure spherical power, cylindrical power, and axis in both eyes. Cycloplegia may be required in children, preferably using 1% tropicamide, one drop each time, three times. Before cycloplegia, check allergy history, medical history, and anterior chamber depth; inform guardians of potential risks and precautions related to cycloplegia, and ensure that guardians accompany the child throughout the procedure.
Questionnairethrough study completion, an average of 1 yearQuestionnaires on demographics, disease histories and etc.
Fundus examinationthrough study completion, an average of 1 yearExamine the retina of both eyes and document any retinal pathology. If pupils are too small, mydriasis may be required, following the same drugs and procedures as above.
Anterior segment examinationthrough study completion, an average of 1 yearUse a slit lamp to examine eyelids, conjunctiva, cornea, anterior chamber, and lens in both eyes. Record any abnormalities. Grade lens opacities according to the LOCS III classification system.

Contacts

Primary ContactLingyi Liang
lianglingyi@gzzoc.com+8602087330487

Outcome results

None listed

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