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ReSure Sealant Post Approval Study — Clinical PAS  

Adverse Events Clinical Trial

Official title:
ReSure Sealant Post-Approval Study: A Registry Evaluation of ReSure Sealant for Specified Adverse Ocular Events After Sealing Corneal Incisions in Patients Undergoing Clear Corneal Cataract Surgery

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

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