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Neovascularization, Pathologic clinical trials

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NCT ID: NCT00729846 Completed - Macular Edema Clinical Trials

Bevacizumab in Combination With Visudyne Photodynamic Therapy (PDT)

Start date: May 2006
Phase: Phase 2
Study type: Interventional

To evaluate safety, visual acuity outcomes, persistence of choroidal neovascular leakage, and the number of treatments of combination intravitreal bevacizumab and verteporfin photodynamic therapy at standard or reduced fluence level in patients with subfoveal CNV due to age-related macular degeneration.

NCT ID: NCT00725686 Completed - Clinical trials for Age-Related Macular Degeneration

Study of PF-04523655 (REDD14NP) In Subjects With Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (Wet AMD)

Start date: February 2007
Phase: Phase 1
Study type: Interventional

The aim of the study is to evaluate whether PF-04523655 is safe in the treatment of neovascular/wet AMD

NCT ID: NCT00685503 Completed - Neovascularization Clinical Trials

Ranibizumab Injections to Treat Macular Telangiectasia With New Blood Vessel Growth

Start date: May 21, 2008
Phase: Phase 1
Study type: Interventional

This study will examine whether the drug ranibizumab (Lucentis) can help prevent vision loss in people with macular telangiectasia, a condition in which new blood vessels grow in the retina at the back of the eye and can leak. Such changes in blood vessels are seen in other diseases associated with changes in a body chemical called vascular endothelial growth factor (VEGF). Ranibizumab is an anti-VEGF drug that is effective in treating another eye disease, age-related macular degeneration, with similar changes in eye blood vessels. People 18 years of age and older with macular telangiectasia in both eyes and new blood vessel growth in at least one eye may be eligible for this study. They must have vision better than 20/400 in the study eye. Participants undergo the following procedures: - Ranibizumab injections in the study eye at least four times over 12 weeks. Depending on the response to treatment and the side effects, additional injections may be given every 4 weeks for up to 1 year. The eye is numbed before the injection and the eye area is cleaned with an antiseptic. Antibiotic drops are used for 3 days following the injection to prevent infection. - Evaluations before starting treatment, at the time of each injection, and 8 weeks after the last treatment: - History and physical examination. - Eye examination with dilation, microperimetry and photography: The eye examination measures visual acuity, eye pressure and eye movements. For the microperimetry test, subjects sit in front of a computer screen and press a button when they see a light on the screen. Measurements and photographs of the retina are also taken. - Fluorescein and indocyanine green angiography to examine the blood vessels in the eye: A dye called fluorescein or indocyanine green is injected into a vein in the arm. The dye travels through the veins to the blood vessels in the eyes. A camera takes pictures of the dye as it flows through the blood vessels. - Pregnancy test: Women who are able to become pregnant have a urine pregnancy test before each ranibizumab injection.

NCT ID: NCT00681889 Completed - Clinical trials for Corneal Neovascularization

Effectiveness and Safety of Topical Ranibizumab for Treatment of Corneal Neovascularization (NV)

Start date: April 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effectiveness and safety of ranibizumab (Lucentis) in treatment of corneal neovascularization.

NCT ID: NCT00677963 Completed - Atherosclerosis Clinical Trials

Contrast-enhanced Ultrasound (CE-US) and Magnetic Resonance Imaging (MRI): Evaluating Plaque Neovascularisation

Start date: June 2009
Phase: N/A
Study type: Interventional

The first goal of this study is to investigate whether CE-US is able to accurately identify and quantify neovascularisation in carotid artery plaques. Since this is one of the first studies systematically evaluating the ability of ultrasound in combination with air bubbles to evaluate neovascularisation in carotid artery plaques, the examination will be performed twice with an interval of 1/2 hour on the day before surgery, thus studying the reliability of the method. The second goal of this study is to investigate whether MRI at 3.0 T with a custom-designed 3T carotid coil, using a recently developed pulse sequence, is able to accurately identify and quantify neovascularisation. And the third goal of this study is to make an intermodality comparison of CE-US and MRI regarding their ability to identify and quantify plaque neovascularisation.

NCT ID: NCT00645697 Completed - Tuberculosis Clinical Trials

Intravitreal Bevacizumab in Recalcitrant Inflammatory Ocular Neovascularization

AVA-ION
Start date: January 2007
Phase: Phase 4
Study type: Observational

One complication of uveitis which is driven by an increase in VEGF is the formation of inflammatory ocular neovascularization (ION). Here, we analyze the therapeutic role of intravitreal bevacizumab in ION not responding to standard therapy (systemic and ocular corticosteroids and systemic immunosuppressants) in a multicenter retrospective study.The natural history of subfoveal choroidal new vessels histoplasmosis, multifocal choroiditis, Harada and other inflammatory chorioretinal disorders has been very guarded, but with this new approach, we hope to stop the visual loss in these relatively young patients.

NCT ID: NCT00606138 Completed - Clinical trials for Proliferative Diabetic Retinopathy

Ranibizumab for Treatment of Persistent Diabetic Neovascularization Assessed by Wide-Field Imaging

Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Diabetic neovascularization refers to a type of diabetic retinopathy which is worsening by the abnormal growth of blood vessels in the back of the eye, damaging the retina. The usual treatment is a type of laser, called panretinal photocoagulation. One drawback is that the amount of space within the eye for use of this treatment eventually has its limit, and should not be used too near the part of the retina used for detailed vision (the macula). In similar eye disorders, there are certain injectable medications called anti-VEGF treatments which can slow down or stop this abnormal blood vessel growth. This study sought to compare use of ranibizumab versus standard panretinal photocoagulation in treatment of diabetic neovascularization.

NCT ID: NCT00604071 Completed - Clinical trials for Age Related Macular Degeneration

Sensitivity of the Home Macular Perimeter (HMP)

HMP
Start date: November 2007
Phase: N/A
Study type: Observational

estimate the sensitivity of the HMP test in identifying visual field functional defects in subjects with CNV secondary to AMD

NCT ID: NCT00570193 Completed - Clinical trials for Macular Degeneration

Photodynamic and Pharmacologic Treatment of CNV

PBS
Start date: December 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this pilot study is to validate the use of the combination of Lucentis (ranibizumab) and Visudyne (verteporfin) in the treatment of choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) and to explore the use of a volumetric analysis of the CNV lesion to determine disease activity, response to therapy, and as a tool for determining the need for retreatment.

NCT ID: NCT00564148 Completed - Clinical trials for Retinal Neovascularization

Intravitreal Avastin in Proliferative Retinopathies

SITE-App
Start date: July 2007
Phase: Phase 2
Study type: Interventional

The study intends to assess the effect of Avastin injections in different proliferative retinopathies due to different causes