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Treatment With Intravitreal Aflibercept Injection For Proliferative Diabetic Retinopathy, The A.C.T Study — ACT  

Proliferative Diabetic Retinopathy Clinical Trial

Official title:
Treatment With Intravitreal Aflibercept Injection For Proliferative Diabetic Retinopathy, The A.C.T Study

Clinical Trial Summary

To assess the safety of intravitreal aflibercept injection in the treatment of proliferative diabetic retinopathy (PDR) by evaluating the incidence and severity of adverse events.

Clinical Trial Description

- Single center, open label pilot study using 2.0mg intravitreal aflibercept injection. (IAI)

- 20 subjects with active PDR to be randomized into 2 groups, i.e. groups A and B.

- Subjects in both arms will be followed-up every 4 weeks until week 52.

- The primary endpoint of the study will be at week 52. ;

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01813773
Study type Interventional
Source Ophthalmic Consultants of Long Island
Contact
Status Completed
Phase Phase 2/Phase 3
Start date March 2013
Completion date April 2016
View Details
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