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NCT01231633 · ClinicalTrials.gov registry record · NA

Comparison of Initial Ozurdex (Dexamethasone Implant) to Avastin (Bevacizumab) for Treatment of Macular Edema Caused by Central Retinal Vein Occlusion (CRVO)

A NA study of Macular Edema and Central Retinal Vein Occlusion, sponsored by Long Island Vitreoretinal Consultants.

Completed
Registry status
NA
Development phase
27
Enrollment target
4
Study locations

NCT01231633 is a NA study of Macular Edema and Central Retinal Vein Occlusion that has completed, run by Long Island Vitreoretinal Consultants. The registered enrollment target is 27 participants, below the 178-participant average among 14 other Macular Edema trials with a reported enrollment target (85% lower). The trial reports 4 study locations across 2 states.

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The verdict

NCT01231633, a NA study of Macular Edema and Central Retinal Vein Occlusion, has completed, sponsored by Long Island Vitreoretinal Consultants.

COMPLETED
Registry status
NA
Development phase
27 participants
Enrollment target
4
Study locations

Study Summary

The purpose of this study is to compare visual improvement and total number of intraocular injections in eyes with macular edema following central retinal vein occlusion (CRVO)after initial treatment with Ozurdex (dexamethasone implant) or Avastin (bevacizumab).

Interventions

  • DRUG Avastin
  • DRUG Ozurdex

Study Locations (4)

New York

  • Long Island Vitreoretinal Consultants - Great Neck
  • Long Island Vitreoretinal Consultants - Hauppauge
  • Long Island Vitreoretinal Consultants - Riverhead

New Jersey

  • Retina Vitreous Center - Toms River

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2010-09
Est. Completion 2014-09
Phase NA

What the Registry Record Tells You About NCT01231633

The ClinicalTrials.gov registry entry for NCT01231633 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 178-participant average among 14 other Macular Edema trials with a reported enrollment target (85% lower). The listed sponsor is Long Island Vitreoretinal Consultants, which has 1 total studies on file at ClinicalTrials.gov.

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

NCT01231633 reports 4 study locations spanning 2 distinct geographic areas - top geographies include New York, New Jersey.

Frequently Asked Questions

What is clinical trial NCT01231633 about?

NCT01231633 is a clinical study titled "Comparison of Initial Ozurdex (Dexamethasone Implant) to Avastin (Bevacizumab) for Treatment of Macular Edema Caused by Central Retinal Vein Occlusion (CRVO)". The purpose of this study is to compare visual improvement and total number of intraocular injections in eyes with macular edema following central retinal vein occlusion (CRVO)after initial treatment with Ozurdex (dexamethasone implant) or Avastin (bevacizumab).

What is the current status of trial NCT01231633?

This trial is currently completed. It is a NA study. The enrollment target is 27 participants. The study started on 2010-09. Estimated completion is 2014-09.

What conditions does trial NCT01231633 study?

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

What interventions are being tested in trial NCT01231633?

The interventions under investigation include: Avastin (DRUG), Ozurdex (DRUG).

Who is sponsoring clinical trial NCT01231633?

This trial is sponsored by Long Island Vitreoretinal Consultants, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01231633 being conducted?

This trial has 4 study locations across New Jersey, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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