Multimodal Risk Prediction Study of Retinal Vascular Occlusion

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2600127033

Enrollment

Unknown

Registered

2026-06-23

Start date

2026-07-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Retinal Vascular Occlusion (RVO)

Interventions

Patients with Retinal Vascular Occlusion:None

Eligibility

Sex/Gender

All

Age

50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for retinal vascular occlusion; 2.Aged between 50 and 80 years old, regardless of gende; 3.Voluntarily sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Patients with other diseases causing fundus lesions; 2.Subjects whose examination results cannot be analyzed;

Design outcomes

Primary

Measure	Time frame
Predictive performance of multimodal risk prediction model for severe clinical outcomes of retinal vascular occlusion;	—

Secondary

Measure	Time frame
Predictive performance of the model for ischemic retinal vascular occlusion;Independent risk factors associated with severe clinical outcomes of retinal vascular occlusion;	—

Countries

China

Contacts

Public ContactChen Xi

Beijing Friendship Hospital ,Capital Medical University

xichen@ccmu.edu.cn+86 10 63138613

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026