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NCT01711879 · ClinicalTrials.gov registry record · NA

Use of Intravitreal Aflibercept Injection for Neovascular Glaucoma

A NA study, sponsored by University of Colorado, Denver.

Completed
Registry status
NA
Development phase
7
Enrollment target

NCT01711879: Completed NA study, sponsored by University of Colorado, Denver.

NCT01711879 is a NA study that has completed, run by University of Colorado, Denver. The registered enrollment target is 7 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01711879, a NA study, has completed, sponsored by University of Colorado, Denver.

COMPLETED
Registry status
NA
Development phase
7 participants
Enrollment target

Study Summary

This 52 week study will assess the use of intravitreal aflibercept injections in patients with neovascular glaucoma (NVG) compared to standard of care panretinal photocoagulation. The investigators hypothesize that the neovascularization of the iris and angle present in neovascular glaucoma will resolve more quickly in eye treated with intravitreal aflibercept injection alone and result in increased comfort and preservation of visual field as compared to current standard of care utilizing pan-retinal photocoagulation. The advantages to intravitreal aflibercept injection use could include resolution of NVI/NVA (neovascularization of the iris/neovascularization of the angle) leading to quicker pain relief and quicker lowering of IOP (intraocular pressure).

Primary Outcome

Assess the safety profile of repeated intravitreal aflibercept injections in patients with NVG by evaluating the incidence of adverse events

Interventions

  • DRUG Aflibercept

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2013-01
Est. Completion 2015-10
Phase NA
University of Colorado, Denver

1,283 total trials

What the finished NCT01711879 record still lists

NCT01711879 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Aflibercept is the first listed.

NCT01711879 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01711879 about?

NCT01711879 is a clinical study titled "Use of Intravitreal Aflibercept Injection for Neovascular Glaucoma". This 52 week study will assess the use of intravitreal aflibercept injections in patients with neovascular glaucoma (NVG) compared to standard of care panretinal photocoagulation. The investigators hypothesize that the neovascularization of the iris and angle present in neovascular glaucoma will re...

What is the current status of trial NCT01711879?

This trial is currently completed. It is a NA study. The enrollment target is 7 participants. The study started on 2013-01. Estimated completion is 2015-10.

What interventions are being tested in trial NCT01711879?

The interventions under investigation include: Aflibercept (DRUG).

Who is sponsoring clinical trial NCT01711879?

This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01711879's enrollment target sits among peer trials

7 1982nd of 2000 higher than 18 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01711879, the US trial registry maintained by the National Library of Medicine. NCT01711879 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.