CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 26 enrolled
Drug / intervention
Aflibercept Ophthalmic +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03022292
NCT03022292Phase 4Completed

The IAI-OCTA Study or; Microvascular Structure and Morphology of Neovascular Membranes in Age Related Macular Degeneration (AMD) After Intravitreal Aflibercept Injection (IAI) Therapy Using OCT-Angiography Analysis

University of California, Los Angeles·interventional·Posted Jan 16, 2017·Updated Jan 6, 2022

In Brief

A Phase 4 clinical trial evaluating Aflibercept Ophthalmic and optovue angiovue for Wet Macular Degeneration. Completed, enrolled 26 participants across 1 site.

Detailed Summary

A study investigating the ability of OCTA imaging technology to identify and analyze untreated type 1, 2, and 3 neovascular membrane lesions in treatment naive patients with exudative macular degeneration, as well as investigating the ability of the OCTA imaging technology to evaluate the treatment outcomes of Intravitreal Aflibercept Injection in neovascular lesions associated with macular degeneration. This study is utilizing a new, FDA approved, non-standard of care technology (OCT-Angiography by Optovue) to image and evaluate the treatment outcomes of using standard of care Intravitreal Aflibercept Injections for their approved use in patients diagnosed with neovascular AMD who are naive to previous Anti-VEGF therapies.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedJan 16, 2017
Enrollment StartMar 30, 2017
Primary CompletionJun 25, 2020
Study CompletionAug 31, 2020
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 9.5 years ago

Interventions

Aflibercept Ophthalmicdrug

IAI given for active exudative macular degeneration (CNV, SRF, PED) per SOC

optovue angiovuedevice

FDA approved Optovue Angiovue will be used to monitor progression and responsiveness of active exudative macular degeneration to IAI.