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Clinical Trial Summary

This is a prospective multicenter observational post-approval registry study that will collect post-approval data relative to the incidence of pre-specified Adverse Ocular Events for cataract surgery patients treated with the FDA-approved ReSure Sealant when used by a broad group of physicians under commercial use conditions.


Clinical Trial Description

n/a


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02310815
Study type Observational
Source Ocular Therapeutix, Inc.
Contact
Status Completed
Phase N/A
Start date December 2014
Completion date April 2016

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