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Early detection and surveillance of COVID-19 infection by non-invasive ophthalmic evaluations

Early detection and surveillance of COVID-19 infection by non-invasive ophthalmic evaluations

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050580
Enrollment
Unknown
Registered
2021-08-29
Start date
2020-08-01
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

Case series:Nil

Sponsors

Food and Health Bureau - Health and Medical Research Fund
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Group 1: (n=30) Confirmed (recently diagnosed) subjects fulfilling laboratory criteria. Group 3: (n=350) Convalescent cases (original strain, 2020)*. Group 4: (n=1600) Subjects with epidemiological link to COVID-19, who meet the CHP reporting criteria of COVID-19, inbound travellers under compulsory quarantine at designated places. Group 5: (n=100) Healthy Subjects with no history of DED or probable/confirmed COVID-19. Group 6a: (n=100) Confirmed (recently diagnosed) subjects fulfilling laboratory criteria (Omicron strain, 2022) recruited from the community. Group 6b: (n=100) Confirmed (recently diagnosed) subjects fulfilling laboratory criteria (Omicron strain, 2022) recruited from hospitals. Group 7: (n=100) Subjects with long-COVID systemic complications. Group 8a: (n=100) Subjects with no history of probable/confirmed COVID-19 and pre-existing primary DED. Group 8b: (n=100) Convalescent subjects with pre-COVID primary DED. Group 9a: (n=100) Subjects with no history of probable/confirmed COVID-19 and pre-existing secondary DED. Group 9b: (n=100) Convalescent subjects with pre-COVID secondary DED.

Exclusion criteria

Exclusion criteria: 1. Mentally not fit for consent; 2. Patients with recent (< 6 months) pneumonia or COVID19 cannot be recruited as healthy control.

Design outcomes

Primary

MeasureTime frame
Descriptive statistics of the clinical, demographic and ophthalmic data;Concordance rate on RT-PCR results between ocular and respiratory samples by Kendall's Coefficient of Concordance;

Secondary

MeasureTime frame
Correlation of ophthalmic data with RT-PCR by mixed linear regression model;Serial viral load changes in positive ocular samples by serial paired t-test;Longitudinal ophthalmic data from patients with positive findings;

Countries

China

Contacts

Public ContactDr Chong Kam Lung Kelvin

Department of Ophthalmology and Visual Sciences, CUHK

chongkamlung@cuhk.edu.hk+852 3943 5805

Outcome results

None listed

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