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Clinical Trial Summary

Specific study objectives include: - To describe patient and provider characteristics for aflibercept patients and aflibercept user injections by aflibercept dispensing device, overall, and stratified by time (quarterly, annually). - To estimate the annual and quarterly incidence of intraocular inflammation (IOI) and suspected endophthalmitis for aflibercept user injections by aflibercept dispensing device. Secondary objectives • To estimate the annual incidence of IOI and suspected endophthalmitis for aflibercept user injections by dispensing device, stratified by indication for use, history of IOI, and provider characteristics.


Clinical Trial Description

This study is entirely descriptive using secondary data from the Vestrum Health Retina Treatment and Outcomes database. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05791695
Study type Observational
Source Regeneron Pharmaceuticals
Contact
Status Completed
Phase
Start date September 16, 2022
Completion date September 15, 2023

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