Aflibercept Injection for Proliferative Diabetic Retinopathy

Status Completed

Clinical Trial Summary

To evaluate the ocular and systemic safety of intravitreal aflibercept injection in patients undergoing Pars Plana Vitrectomy for Proliferative Diabetic Retinopathy.

Clinical Trial Description

Patients who need Pars Plana Vitrectomy surgery, and agree to participate in this study will receive an injection of 2.0mg aflibercept 4 to 6 days before Vitrectomy surgery. Half of these patients will be randomized to receive another injection of 2.0mg aflibercept immediately after their surgery. Postoperative patient visits in this study will be at 1 day, and at weeks 1, 4, 16 and 24, and at any other times as deemed necessary by the Investigator. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01805297
Study type	Interventional
Source	University of Oklahoma
Contact
Status	Completed
Phase	Phase 2
Start date	March 2013
Completion date	November 2015

View Details

See also
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