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NCT00370851

Intravitreal Bevasizumab VS Sham Treatment in Acute BRVO: A Randomized Clinical Trial

Completed Phase 3 Last updated 23 November 2009
What this trial tests

Phase 3 trial testing Avastin (Bevacizumab) in Retinal Disease in 82 participants. Completed in 1 June 2008.

Timeline
1 August 2006
Primary endpoint
1 February 2008
1 June 2008

Quick facts

Lead sponsorShahid Beheshti University of Medical Sciences
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment82
Start date1 August 2006
Primary completion1 February 2008
Estimated completion1 June 2008
Sites1 location across Iran

Drugs / interventions tested

Conditions studied

Sponsor

Shahid Beheshti University of Medical Sciences

Who can join

40 and older, any sex, with Retinal Disease. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

In this study we intend to evaluate the outcome of intravitreal avastin on improving the visual acuity and macular edema and late complications of BRVO like NVD and NVE

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A systematic review and meta-analysis of the effect of intravitreal VEGF inhibitors on cardiorenal outcomes.
    Lees JS, Dobbin SJH, Elyan BMP, Gilmour DF, et al · · 2023 · cited 12× · PMID 36318455 · DOI 10.1093/ndt/gfac305

Verify or expand the search:

Other recruiting trials for Retinal Disease

Currently open trials in the same condition.

Other Shahid Beheshti University of Medical Sciences trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00370851.

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