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NCT00406107 · ClinicalTrials.gov registry record · Phase 4

Evaluation of Macugen Treatment of Macular Edema Due to Branch Retinal Vein Occlusion

A Phase 4 study of Branch Retinal Vein Occlusion, sponsored by Palmetto Retina Center.

Completed
Registry status
Phase 4
Development phase
20
Enrollment target
3
Study locations

NCT00406107: Completed Phase 4 study of Branch Retinal Vein Occlusion, sponsored by Palmetto Retina Center.

NCT00406107 is a Phase 4 study of Branch Retinal Vein Occlusion that has completed, run by Palmetto Retina Center. The registered enrollment target is 20 participants, below the 2,065-participant average among 3 other Branch Retinal Vein Occlusion trials with a reported enrollment target (99% lower). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00406107, a Phase 4 study of Branch Retinal Vein Occlusion, has completed, sponsored by Palmetto Retina Center.

COMPLETED
Registry status
Phase 4
Development phase
20 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this study is to evaluate the effect of intravitreal injections of Macugen every 6 weeks for the treatment of macular edema secondary to branch retinal vein occlusion (BRVO). We hypothesize that macular edema secondary to BRVO is mediated by VEGF 165 and that chronic suppression of VEGF 165 will successfully treat BRVO related macular edema.

Interventions

  • DRUG pegaptanib sodium (Macugen)

Study Locations (3)

California

  • Jules Stein Eye Institute - Los Angeles

Maryland

  • Cumberland Valley Retina Center - Hagerstown

South Carolina

  • Palmetto Retina Center - West Columbia

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2006-01
Est. Completion 2008-04
Phase Phase 4
Palmetto Retina Center

2 total trials

What the finished NCT00406107 record still lists

NCT00406107 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 2,065-participant average among 3 other Branch Retinal Vein Occlusion trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Branch Retinal Vein Occlusion appearing as the primary indexed condition, and to 1 intervention - of which pegaptanib sodium (Macugen) is the first listed.

NCT00406107 reports a single indexed study location in California, Maryland, South Carolina.

Frequently Asked Questions

What is clinical trial NCT00406107 about?

NCT00406107 is a clinical study titled "Evaluation of Macugen Treatment of Macular Edema Due to Branch Retinal Vein Occlusion". The purpose of this study is to evaluate the effect of intravitreal injections of Macugen every 6 weeks for the treatment of macular edema secondary to branch retinal vein occlusion (BRVO). We hypothesize that macular edema secondary to BRVO is mediated by VEGF 165 and that chronic suppression of VE...

What is the current status of trial NCT00406107?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2006-01. Estimated completion is 2008-04.

What conditions does trial NCT00406107 study?

This clinical trial studies the following conditions: Branch Retinal Vein Occlusion.

What interventions are being tested in trial NCT00406107?

The interventions under investigation include: pegaptanib sodium (Macugen) (DRUG).

Who is sponsoring clinical trial NCT00406107?

This trial is sponsored by Palmetto Retina Center, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00406107 being conducted?

This trial has 3 study locations across California, Maryland, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00406107, the US trial registry maintained by the National Library of Medicine. NCT00406107 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.