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NCT01428388 · ClinicalTrials.gov registry record · NA

Bevacizumab Versus Ranibizumab in Treatment of Macular Edema From Vein Occlusion

A NA study of Macular Edema and Retinal Vein Occlusion, sponsored by Barnes Retina Institute.

Completed
Registry status
NA
Development phase
150
Enrollment target
1
Study location

NCT01428388: Completed NA study of Macular Edema and Retinal Vein Occlusion, sponsored by Barnes Retina Institute.

NCT01428388 is a NA study of Macular Edema and Retinal Vein Occlusion that has completed, run by Barnes Retina Institute. The registered enrollment target is 150 participants, below the 169-participant average among 14 other Macular Edema trials with a reported enrollment target (11% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01428388, a NA study of Macular Edema and Retinal Vein Occlusion, has completed, sponsored by Barnes Retina Institute.

COMPLETED
Registry status
NA
Development phase
150 participants
Enrollment target
1
Study location

Study Summary

Antagonists of the vascular endothelial growth factor (VEGF) pathway are effective in treating macular edema resulting from retinal vein occlusion (RVO). In the eye, the two most widely used anti-VEGF agents are ranibizumab and bevacizumab. Only ranibizumab has been FDA-approved for the treatment of macular edema from RVO, however bevacizumab has been used off-label by many ophthalmologists with good success. Furthermore, the cost of bevacizumab is less than one-tenth the cost of ranibizumab. Here the investigators conduct a six month randomized, prospective interventional trial comparing the effectiveness of ranibizumab with bevacizumab in the treatment of macular edema from RVO. Primary outcome measures are change in central retinal thickness. Secondary measures are change in visual acuity from baseline and change in angiographic properties of macular lesions from baseline after treatment.

Primary Outcome

central thickness is measured using optical coherence tomography (OCT)

Interventions

  • DRUG Intravitreal injection of bevacizumab
  • DRUG Intravitreal injection of ranibizumab (0.5 mg per dose)

Study Locations (1)

Missouri

  • The Retina Institute - St Louis

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2011-09
Est. Completion 2015-12
Phase NA
Barnes Retina Institute

6 total trials

What the finished NCT01428388 record still lists

NCT01428388 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 169-participant average among 14 other Macular Edema trials with a reported enrollment target (11% lower).

The record links to 2 conditions, with Macular Edema appearing as the primary indexed condition, and to 2 interventions - of which Intravitreal injection of bevacizumab is the first listed.

NCT01428388 reports a single indexed study location in Missouri.

Frequently Asked Questions

What is clinical trial NCT01428388 about?

NCT01428388 is a clinical study titled "Bevacizumab Versus Ranibizumab in Treatment of Macular Edema From Vein Occlusion". Antagonists of the vascular endothelial growth factor (VEGF) pathway are effective in treating macular edema resulting from retinal vein occlusion (RVO). In the eye, the two most widely used anti-VEGF agents are ranibizumab and bevacizumab. Only ranibizumab has been FDA-approved for the treatment of...

What is the current status of trial NCT01428388?

This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2011-09. Estimated completion is 2015-12.

What conditions does trial NCT01428388 study?

This clinical trial studies the following conditions: Macular Edema, Retinal Vein Occlusion.

What interventions are being tested in trial NCT01428388?

The interventions under investigation include: Intravitreal injection of bevacizumab (DRUG), Intravitreal injection of ranibizumab (0.5 mg per dose) (DRUG).

Who is sponsoring clinical trial NCT01428388?

This trial is sponsored by Barnes Retina Institute, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01428388 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Macular Edema

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01428388's enrollment target sits among peer trials

150 6th of 14 higher than 9 of 14 other Macular Edema trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Macular Edema 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 NCT01428388, the US trial registry maintained by the National Library of Medicine. NCT01428388 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.