Assessment of Patients Treated With JETREA® for Vitreomacular Traction

Status Completed

Clinical Trial Summary

The purpose of this study is to observe the anatomical and functional outcomes of ocriplasmin (JETREA®) over a 6-month follow-up period.

Clinical Trial Description

Subjects will be recruited from approximately 90 centers in approximately 11 countries across Europe and Canada. After receiving a single intravitreal injection as per country's product label (Day 0), subjects will be followed for a 6-month period (Day 180). ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02035748
Study type	Interventional
Source	Alcon Research
Contact
Status	Completed
Phase	Phase 4
Start date	April 2014
Completion date	September 2015

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