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OTX-14-002: Device Exposure Registry

Endophthalmitis Clinical Trial

Official title:
Device Exposure Registry: A Post-Approval Observational Registry of ReSure Sealant to Track the Incidence of Endophthalmitis After Sealing Corneal Incisions in Patients Undergoing Clear Corneal Cataract Surgery

Clinical Trial Summary

The objective of the study is to collect post-approval data relative to the incidence of endophthalmitis 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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02309736
Study type Observational
Source Ocular Therapeutix, Inc.
Contact
Status Withdrawn
Phase
View Details
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