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Active clinical trials for "Macular Degeneration"

Results 661-670 of 1337

A Study to Evaluate the Safety and Clinical Response of Subretinal Administration of CNTO 2476 in...

Visual AcuityGeographic Atrophy1 more

The purpose of this study is to evaluate the safety and performance profile of the suprachoroidal surgical approach and the Delivery System.

Completed9 enrollment criteria

Anesthesia Preference for Intravitreal Injection: Topical or Subconjunctival

Age-related Macular DegenerationCentral Retinal Vein Occlusion1 more

Since 2004, intravitreal injection of Avastin, Lucentis, and Macugen for wet age-related macular degeneration, retinal vein occlusion, and diabetic macular edema are being administered in the United States at increasing rates. A 2010 study showed that in Canada and the incidence of injections grew 8 fold from 2005 to 2007 to 25.9 injections per 100,000 citizens. (Campbell 2010) In 2009, in the United States, over 1 million intravitreal injections were administered to Medicare beneficiaries. (Wykoff 2011) In the year 2011, the four doctors in my retina group administered a total of 6,494 intravitreal injections; in 2010, we administered 5021 intravitreal injections. Even though intravitreal injections are commonly administered, the optimal method of anesthetizing the eye prior to injection has yet to be determined. Some physicians use an anesthetic drop, some a soaked cotton pledget, some use an anesthetic gel and some use subconjunctival injected anesthetic. In 2009, the last time the Procedures and Trends Survey (PAT) (Mittra 2009) conducted by the American Society of Retina Specialists (the largest retina society in the world) asked about anesthetic methods for administering intravitreal injections, the following response was given by the 433 respondents: Topical anesthetic drop: 21.48% Topical viscous anesthetic: 23.33% Topical anesthetic & soaked cotton-tip or pledget: 29.79% Subconjunctival injection of anesthetic: 24.02% Other: 1.39% An editorial in 2011 in the journal Retina, discusses the lack of good studies assessing optimal anesthetic prior to intravitreal injections. (Prenner 2011).

Completed4 enrollment criteria

Wet Macular Degeneration Study to Compare Ranibizumab or Bevacizumab to Aflibercept

Exudative Macular Degeneration

This study will examine the use of Aflibercept in patients with exudative macular degeneration requiring intravitreal injections. Patients will be followed for 24 months. The follow up phase will be completed at month 36.

Completed43 enrollment criteria

ESBA1008 Microvolume Study

Exudative Age-Related Macular Degeneration

The purpose of this study is to demonstrate a treatment effect of ESBA1008 applied as a microvolume injection or infusion on retinal function and morphology in subjects with exudative age-related macular degeneration (AMD).

Completed17 enrollment criteria

Safety Study of a Topical Treatment for Dry Age Related Macular Degeneration

Nonexudative Age-related Macular Degeneration

Study to evaluate the safety and tolerability of MC-1101, a potential topical treatment for non-edxudative age Related Macular Degeneration (AMD) in medically stable individuals.

Completed27 enrollment criteria

Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-related Macular Degeneration...

Macular Degeneration

This is a safety and efficacy study of abicipar pegol in participants with neovascular age-related macular degeneration.

Completed5 enrollment criteria

Study of the Efficacy and Safety of the Ranibizumab Port Delivery System for Sustained Delivery...

Macular Degeneration

This is a Phase II multicenter, dose-ranging, randomized, active treatment (monthly ITV injection)-controlled study to evaluate the efficacy, safety, and pharmacokinetics of ranibizumab delivered through the Implant using three ranibizumab formulation arms (10 mg/mL, 40 mg/mL, and 100 mg/mL) compared with the control arm (0.5-mg monthly ITV injections of 10-mg/mL formulation) in participants with subfoveal neovascular age-related macular degeneration (nAMD).

Completed23 enrollment criteria

A Safety and Efficacy Study of DE-120 Injectable Solution for Age-related Macular Degeneration

Age-Related Macular Degeneration

The purpose of the study is to evaluate the safety and efficacy of intravitreal (IVT) administration of DE-120 in subjects with treatment-naive active subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD).

Completed21 enrollment criteria

Ozurdex for Macular Edema Post Membrane Peeling

Epiretinal MembraneCellophane Maculopathy2 more

An epiretinal membrane is scar tissue on the retina that can cause blurring and distortion of vision and lead to swelling, or macular edema. Despite surgery to remove the scar tissue(membrane peeling), residual swelling of the retina may continue to interfere with vision. In this study the investigators will inject an implantable steroid device into the back, fluid-filled portion of the eye. Steroids have been found to decrease the swelling in the retina. Ozurdex™ is an implantable steroid. Once implanted, Ozurdex™ is slowly dissolved by the vitreous gel that fills the eye, releasing the steroid. The steroid drug delivery system in this study, known as Ozurdex™ has been FDA-approved by the US Food and Drug Administration (FDA) for decreasing swelling due to another condition in the eye. This study will help to find out whether or not this device Ozurdex™ is also effective for reducing the swelling of the retina in patients who have already had surgery to remove scar tissue on the retina.

Completed13 enrollment criteria

Phase I Dose Escalation Safety Study of RetinoStat in Advanced Age-Related Macular Degeneration...

Age Related Macular Degeneration

The purpose of this first in man study is to examine the safety of an experimental gene transfer agent, RetinoStat, designed to treat neovascular age-related macular degeneration.

Completed7 enrollment criteria
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