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Macular Degeneration clinical trials

View clinical trials related to Macular Degeneration.

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NCT ID: NCT00733304 Completed - Clinical trials for Macular Degeneration

An Extension to Study MD7108240

Start date: June 25, 2008
Phase: Phase 2
Study type: Interventional

This is a two month study to allow continued treatment with pazopanib eye drops. Study may be extended to 5 months.

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: NCT00727753 Completed - Clinical trials for Macular Degeneration

VEGF-antagonism and Endothelial Function in Age-related Macular Degeneration (AMD)

Start date: July 2008
Phase: Phase 4
Study type: Observational

The objective of this study is to evaluate the effects of 2 intravitreal injections with Ranibizumab or Avastin on endothelial function in subjects with neovascular macular degeneration compared to patients with dry AMD.

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: NCT00722384 Completed - Clinical trials for Macular Degeneration

Open Label Study for the Evaluation of Tolerability of Five Dose Levels of Cand5

Start date: August 2004
Phase: Phase 1
Study type: Interventional

To establish the tolerability and preliminary efficacy of Cand5 by a single intravitreal injection in patients with wet age-related macular degeneration.

NCT ID: NCT00713518 Completed - Clinical trials for Age Related Macular Degeneration

Phase II Open Label Multicenter Study For Age Related Macular Degeneration Comparing PF-04523655 Versus Lucentis In The Treatment Of Subjects With CNV (MONET Study).

MONET
Start date: November 2009
Phase: Phase 2
Study type: Interventional

The aim of the study is to evaluate whether PF-04523655 is effective in the treatment of neovascular/wet AMD and at which dose.

NCT ID: NCT00709527 Completed - Clinical trials for Age-Related Macular Degeneration

ARC1905 (ANTI-C5 APTAMER) Given Either In Combination Therapy With Lucentis® 0.5 mg/Eye In Subjects With Neovascular Age-Related Macular Degeneration

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

The objectives of this study are to evaluate the safety, tolerability, and pharmacokinetic profile of multiple doses of ARC1905 intravitreous injection when administered in combination with multiple doses of Lucentis® 0.5 mg/eye, or with one induction dose of Lucentis 0.5 mg/eye in subjects with subfoveal choroidal neovascularization secondary to age-related macular degeneration (AMD).

NCT ID: NCT00709449 Completed - Glaucoma Clinical Trials

An Open Study Comparing the Effects of Moxaverine on Ocular Blood Flow in Patients With Age- Related Macular Degeneration, Primary Open Angle Glaucoma and Healthy Control Subjects

Start date: May 2008
Phase: Phase 2/Phase 3
Study type: Interventional

A number of common eye diseases such as age-related macular degeneration and glaucoma are associated with ocular perfusion abnormalities. Although this is well recognized there is not much possibility to improve blood flow to the posterior pole of the eye in these diseases. For many years, moxaverine has been used in the therapy of perfusion abnormalities in the brain, the heart and the extremities. This is based on a direct vasodilatatory effect of the drug, but also on the rheological properties of red blood cells. In a recent study the investigators have shown that intravenous moxaverine increases choroidal blood flow in healthy young subjects. The present study aims to investigate, whether moxaverine also improves blood flow in the diseased eye after systemic administration.

NCT ID: NCT00708929 Completed - Clinical trials for Macular Degeneration

Does Complement Factor H Gene Polymorphism Play a Role in the Regulation of Vascular Tone in the Choroid?

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

Age related macular degeneration (AMD) is a multifactorial disease with a strong genetic component. Most importantly a genetic polymorphism in the gene encoding for the complement factor H (CFH) has been recently identified which is highly associated with an increased risk of developing AMD. This Tyr402His polymorphism located on chromosome 1q31 has been implicated to play a role in the development of the disease. Given that it is known that impaired regulation of choroidal vascular tone is present in patients with AMD, the current study seeks to investigate whether the Tyr402His polymorphism is associated with altered choroidal autoregulation in healthy subjects. For this purpose a total of 100 healthy volunteers will be included in order to test the hypothesis that an impaired regulation of choroidal blood flow is present in subjects with homozygous Tyr402His variant.

NCT ID: NCT00692887 Completed - Clinical trials for Age Related Macular Degeneration

Correlation Between Visual Field Defects on Foresee Preferential Hyperacuity Perimeter(PHP) and on Optical Coherence Tomography (OCT) in Patients With Choroidal Neovascularization (CNV)

PHP
Start date: June 2008
Phase: N/A
Study type: Observational

Study come to investigate the correlation between visual fields (VF) defects map generated by preferential hyperacuity perimeter (PHP) and features of the choroidal neovascular lesions (CNV) demonstrated by Optical Coherence Tomography(OCT). To investigate the Foresee PHP ability to asses treatment progression post treatment.