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Central Retinal Vein Occlusion clinical trials

View clinical trials related to Central Retinal Vein Occlusion.

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NCT ID: NCT00567697 Completed - Macular Edema Clinical Trials

A Randomized Study Comparing Ranibizumab to Sham in Patients With Macular Edema Secondary to CRVO

Start date: March 2007
Phase: Phase 3
Study type: Interventional

A prospective multicenter study comparing patients with CRVO amd secondary macular edema treated with ranibizumab versus sham. Safety and efficacy will be evaluated. Patients will be randomized in a 1:1 ratio to one of the two arms. 32 patients, 6 months follow up. There will be monthly visits with injection the first three months and subsequently new injection if present edema.

NCT ID: NCT00556114 Completed - Glaucoma Clinical Trials

A Pilot Study of Functional Optical Coherence Tomography for Ocular Imaging

Start date: January 2007
Phase:
Study type: Observational

Growing evidence shows that altered blood flow plays a major role in many vision-threatening diseases including glaucoma, diabetic retinopathy, age-related macular degeneration, Central Retinal Vein Occlusion, and Branch Retinal Vein Occlusion. Optical coherence tomography, an established imaging technique use for eye exam in clinical ophthalmology, provides high-resolution cross sectional images of the retina and has increased our ability to understand many eye diseases.

NCT ID: NCT00532142 Completed - Clinical trials for Central Retinal Vein Occlusion

The ROVO Study: Radial Optic Neurotomy for CVO

Start date: April 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The ROVO study is a prospective, placebocontrolled and randomised study designed to evaluate the effect of radial optic neurotomy in central vein occlusion, versus triamcinolone acetonide. 240 patients with a visual acuity < 0.5 Snellen will be randomised. Patients are treated with either RON, or a single intravitreal injection of 4 mg triamcinolone acetonide, or a placebo treatment - a "sham" injection of intravitreal triamcinolone. Patients will be examined regularly over a period of one year. Best corrected visual acuity for far and near, as well as clinical examinations, fluorescein- and indocyanine green angiograms, optical coherence tomography, and perimetry, are performed pre- and postoperatively.

NCT ID: NCT00406796 Completed - Clinical trials for Central Retinal Vein Occlusion

Lucentis for Central Retinal Vein Occlusion (CRVO)

Start date: January 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether ranibizumab will be effective in reducing if not eliminating the macular edema associated with the disease, central retinal vein occlusion (CRVO).