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Retrospective Study of the Safety and Efficacy of Patients With RVO in Subjects Who Completed Parent Study CLS1003-201

Macular Edema Clinical Trial

Official title:
Retrospective Study of the Safety and Efficacy of Suprachoroidal CLS-TA in Combination With Intravitreal Aflibercept for the Treatment of Macular Edema Associated With RVO in Subjects Who Completed Parent Study CLS1003-201

Clinical Trial Summary

The purpose of this non interventional retrospective study is to continue to collect data from patients following their completion of Protocol CLS 1003-201: "Safety and Efficacy of Suprachoroidal CLS-TA with Intravitreal Aflibercept in Subjects with Macular Edema Following Retinal Vein Occlusion" (ie, the parent study).

Clinical Trial Description

This is a non-interventional, retrospective study of up to 6 months for subjects that completed the parent study CLS1003-201. This study is designed to collect data from patients following their parent study exit visit, through either the time of the next treatment for RVO or at least 6 months following the parent study exit visit, whichever occurs first.

During this non-interventional retrospective study, the following data will be collected in an online questionnaire (or where required, on paper) provided by Clearside:

- Next RVO therapy administered (if applicable), including reason for treatment

- Continued documentation of current or changes in medical or ocular conditions following parent study

- Concomitant drug or therapy changes

- Visual acuity, including details on the method used in the assessment

- Central retinal thickness, including details on the equipment used in its determination

- Intraocular pressure, including details on the equipment used in its determination

Subjects will be selected based on parent study primary investigator's access to their medical records access, following exit from CLS1003-201. Data will also be collected on the total number of patients included in this non interventional study as well as reasons patients were excluded. Data will be summarized from the randomization treatment assignment in the parent study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02956330
Study type Observational
Source Clearside Biomedical, Inc.
Contact
Status Completed
Phase
Start date November 2016
Completion date April 12, 2017
View Details
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