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NCT00593450 · ClinicalTrials.gov registry record · Phase 3

Comparison of Age-related Macular Degeneration Treatments Trials: Lucentis-Avastin Trial

A Phase 3 study of Age-related Macular Degeneration, sponsored by University of Pennsylvania.

Completed
Registry status
Phase 3
Development phase
1,208
Enrollment target
20
Study locations

NCT00593450: Completed Phase 3 study of Age-related Macular Degeneration, sponsored by University of Pennsylvania.

NCT00593450 is a Phase 3 study of Age-related Macular Degeneration that has completed, run by University of Pennsylvania. The registered enrollment target is 1,208 participants, below the 1,491-participant average among 74 other Age-related Macular Degeneration trials with a reported enrollment target (19% lower). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00593450, a Phase 3 study of Age-related Macular Degeneration, has completed, sponsored by University of Pennsylvania.

COMPLETED
Registry status
Phase 3
Development phase
1,208 participants
Enrollment target
20
Study locations

Study Summary

The purpose of the study is to evaluate the relative efficacy and safety of treatment of neovascular AMD with Lucentis on a fixed schedule, Avastin on a fixed schedule, Lucentis on a variable schedule, and Avastin on a variable schedule. A five year follow-up visit is being conducted in 2014 to gather information on long term outcomes.

Primary Outcome

Visual acuity testing was performed with the Electronic Visual Tester (EVA) following the ETDRS protocol. VA score is measured as number of letters read correctly. The VA score change is the difference of the VA score at 1 Year and the VA score at baseline. In this study, the outcome VA score change is ranged from -71 to 52, with the higher VA score change the better visual acuity improvement.

Interventions

  • DRUG bevacizumab
  • DRUG ranibizumab

Study Locations (20)

California

  • California Retina Consultants - Bakersfield
  • Retina-Vitreous Associates Medical Group - Beverly Hills
  • University of California-Davis Medical Center - Sacramento
  • Retinal Consultants Medical Group, Inc. - Sacramento
  • West Coast Retina Medical Group, Inc. - San Francisco
  • California Retinal Consultants - Santa Barbara
  • West Coast Retina Medical Group, Inc. - Walnut Creek

Arizona

  • Retina Consultants of Arizona - Mesa
  • Retinal Consultants of Arizona - Phoenix
  • Retina Associates Southwest, P.C. - Tucson

Illinois

  • Illinois Retina Associates - Flossmoor
  • Ingalls Memorial Hospital/Illinois Retina Associates - Harvey
  • Illinois Retina Associates - Joliet

Florida

  • Retina Group of Florida - Fort Lauderdale
  • National Ophthalmic Research Institute - Fort Myers

Colorado

  • Colorado Retina Associates - Denver

Georgia

  • Emory Eye Center - Atlanta

Indiana

  • Midwest Eye Institute - Indianapolis

Iowa

  • University of Iowa Hospitals and Clinics - Iowa City

Trial Details

FieldValue
Enrollment Target 1,208 participants
Start Date 2008-02
Est. Completion 2015-04
Phase Phase 3
University of Pennsylvania

1,423 total trials

What the finished NCT00593450 record still lists

NCT00593450 is an interventional study that assigns participants to a tested intervention. Its 1,208 participants enrollment target places it among the larger protocols in the corpus, below the 1,491-participant average among 74 other Age-related Macular Degeneration trials with a reported enrollment target (19% lower).

The record links to 1 condition, with Age-related Macular Degeneration appearing as the primary indexed condition, and to 2 interventions - of which bevacizumab is the first listed.

NCT00593450 names 20 study sites across 9 states, led by California, Arizona, Illinois.

Frequently Asked Questions

What is clinical trial NCT00593450 about?

NCT00593450 is a clinical study titled "Comparison of Age-related Macular Degeneration Treatments Trials: Lucentis-Avastin Trial". The purpose of the study is to evaluate the relative efficacy and safety of treatment of neovascular AMD with Lucentis on a fixed schedule, Avastin on a fixed schedule, Lucentis on a variable schedule, and Avastin on a variable schedule. A five year follow-up visit is being conducted in 2014 to gat...

What is the current status of trial NCT00593450?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,208 participants. The study started on 2008-02. Estimated completion is 2015-04.

What conditions does trial NCT00593450 study?

This clinical trial studies the following conditions: Age-related Macular Degeneration.

What interventions are being tested in trial NCT00593450?

The interventions under investigation include: bevacizumab (DRUG), ranibizumab (DRUG).

Who is sponsoring clinical trial NCT00593450?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00593450 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Age-related Macular Degeneration

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 NCT00593450's enrollment target sits among peer trials

1,208 4th of 74 higher than 71 of 74 other Age-related Macular Degeneration trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Age-related Macular Degeneration 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 NCT00593450, the US trial registry maintained by the National Library of Medicine. NCT00593450 (large enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.