Cohort study of patients with uveitis
The Cohort Study of Uveitis Patients Based on Real-world Data
This study is trying to learn more about uveitis, including how it affects people's eyes and vision, to find the best ways to diagnose and treat it.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 600 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Zhongshan Ophthalmic Center, Sun Yat-sen University Academic / other |
| Locations | 1 site (Guangzhou, Guangdong) |
| Trial ID | NCT05727540 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the epidemiology, pathogenesis, clinical manifestations, diagnosis, and treatment of uveitis. By collecting real-world data, the study seeks to assess the activity of inflammation and visual prognosis in uveitis patients. The ultimate goal is to establish optimal diagnostic and treatment protocols for managing uveitis effectively.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with uveitis who agree to participate.
Not a fit: Patients who have uveitis within the first month after intraocular surgery, those under 18 years old, pregnant or lactating women, and individuals with other unsuitable conditions will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved diagnosis and treatment strategies for patients suffering from uveitis.
How similar studies have performed: While this study focuses on real-world data, similar cohort studies in uveitis have shown promise in understanding the condition better, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * The diagnosis is uveitis; The agreement of enrolling this study; Exclusion Criteria: * Uveitis during the first month after any intraocular surgery; \<18 years; pregnant and lactating women; other conditions are unsuitable for participation in this study by the investigator such as mental abnormalities.
Where this trial is running
Guangzhou, Guangdong
- Zhongshan Ophthalmic Center — Guangzhou, Guangdong, China (Recruiting)
Study contacts
- Study coordinator: Ye Dai, doctor
- Email: daiye@gzzoc.com
- Phone: 13512721192
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.