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Completed Phase 1 Interventional

Lucentis for Central Retinal Vein Occlusion (CRVO)

ClinicalTrials.gov ID: NCT00406796

Public ClinicalTrials.gov record NCT00406796. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 10:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

FVF3565s Intravitreal Ranibizumab (rhuFab V2) in the Treatment of Macular Edema Associated With Perfused Central (CRVO) Retinal Venous Occlusive Disease

Study identification

NCT ID
NCT00406796
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
California Retina Consultants
Other
Enrollment
20 participants

Conditions and interventions

Interventions

  • Ranibizumab Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2005
Primary completion
Aug 31, 2008
Completion
Sep 30, 2010
Last update posted
Dec 11, 2013

2006 – 2010

United States locations

U.S. sites
4
U.S. states
1
U.S. cities
4
Facility City State ZIP Site status
California Retina Consultants Bakersfield California 93309
California Retina Consultants Oxnard California 93030
California Retina Consultants Santa Barbara California 93103
California Retina Consultants Santa Maria California 93454

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00406796, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 11, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00406796 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →