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Epiretinal Membrane clinical trials

View clinical trials related to Epiretinal Membrane.

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NCT ID: NCT01273727 Completed - Macular Edema Clinical Trials

Ozurdex for Macular Edema Post Membrane Peeling

Start date: June 2010
Phase: Phase 2/Phase 3
Study type: Interventional

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.

NCT ID: NCT01238393 Completed - Epiretinal Membrane Clinical Trials

Treatment of Epiretinal Membranes With Ranibizumab

LERM
Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether intraocular injection of ranibizumab decreases the retinal thickness in patients with epiretinal membranes and reduces associated symptoms.

NCT ID: NCT01162356 Completed - Glaucoma Clinical Trials

Prospective Retinal and Optic Nerve Vitrectomy Evaluation (PROVE) Study

PROVE
Start date: July 2010
Phase: N/A
Study type: Observational

Since the introduction of vitrectomy in 1971, this procedure has become the third most frequently performed ophthalmic surgery. Approximately 225,000 vitrectomies are performed annually in the United States and indications continue to expand. Known long-term complications of vitrectomy are relatively few and include retinal detachment and cataract formation. Although much has been written in the literature concerning acute rises in intraocular pressure (IOP) in the immediate postoperative period, there is surprisingly little information on long term IOP outcomes after vitrectomy. A recent report by Chang given at the LXII (62) Edward Jackson Memorial Lecture hypothesized a causal relationship between vitrectomy and open-angle glaucoma (OAG) via oxidative stress exacerbated by removal of the crystalline lens. A second report by Luk and colleagues reported similar conclusions in a modified cohort. Both studies, were retrospective in nature and did not perform baseline evaluations to exclude pre-existing glaucoma. Furthermore neither study accounted for natural history. Finally, our analysis has not reproduced similar results. The primary purpose of this study is to analyze the full spectrum of optic nerve and macular changes between vitrectomized study eyes and their non-vitrectomized fellow eyes to control for natural history. Baseline evaluations will include examination by fellowship trained retina and glaucoma specialists, fundus photography, autofluorescence, optical coherence tomography (macula and optic nerve) and automated visual field testing. At 3 month then annually for 5 years after vitrectomy surgery, the cohort will undergo similar evaluation.

NCT ID: NCT00974753 Completed - Macular Edema Clinical Trials

Prophylactic Ketorolac Post Epiretinal Membrane Surgery

Start date: March 2010
Phase: N/A
Study type: Interventional

Evaluate the efficacy of ketorolac 0.5%, a topical non-steroidal anti-inflammatory drug (NSAID), to prevent macular edema after epiretinal membrane surgery. Patients undergoing epiretinal membrane surgery have increased risk of macular swelling which can adversely affect vision. Since post-intraocular surgery inflammation is a contributing factor to macular swelling and loss of vision, NSAID drops may be able to prevent or minimize the deleterious effects of macular swelling after epiretinal membrane surgery.

NCT ID: NCT00902629 Completed - Epiretinal Membrane Clinical Trials

Epiretinal Fibrosis, Effect of Early Surgery

epitell
Start date: May 2008
Phase: N/A
Study type: Interventional

The goal of this randomized clinical trial is to investigate when it is optimal to treat the eye disease epiretinal fibrosis. Hypothesis: In a population of patients with symptomatic idiopathic epiretinal fibrosis and visual acuity above 0.4, the best long term outcome measured by visual acuity is achieved by early surgery compared to periodic controls until a continual loss of visual acuity has been ensure followed by surgery.

NCT ID: NCT00818844 Completed - Epiretinal Membrane Clinical Trials

Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the macular volume of patients treated with a 3-month course of topical Nepafenac (0.1% solution) to patients treated with a placebo course following epiretinal membrane surgery.

NCT ID: NCT00757380 Completed - Clinical trials for Idiopathic Epiretinal Membranes

Trypan Blue Versus Brillant Blue for Epiretinal Membranes

Start date: July 2008
Phase: N/A
Study type: Interventional

Membraneppeling alone versus Membranepeeling with Membrane Limitans Interna Pelling using two different Dyes for Epiretinal Membrane Surgery.

NCT ID: NCT00555269 Completed - Macular Hole Clinical Trials

Membrane Blue Versus Infracyanine Green

Start date: October 2004
Phase: N/A
Study type: Observational

To compare possible toxicities of membrane blue and infracyanine green in vivo by macular function and peripheral visual field.

NCT ID: NCT00537992 Completed - Cataract Clinical Trials

Blue-Blocking IOLs in Combined Surgery

Start date: October 2004
Phase: N/A
Study type: Interventional

Although commonly used in cataract surgery, the use of the blue light-filter IOLs in vitrectomy combined with cataract surgery has not been reported yet. A prospective controlled clinical trial was designed to evaluate the effect of the blue light-filter IOL on the surgeon's ability to perform specific vitreoretinal procedures and on the patients' outcome.

NCT ID: NCT00437593 Completed - Retinal Diseases Clinical Trials

UHR-OCT and HD-OCT for Preretinal Membranes: ICG Versus Membrane Blue

Start date: September 2005
Phase: N/A
Study type: Interventional

Using the UHR-OCT and HD-OCT to evaluate early postoperative changes in patients with diagnosis preretinal membrane after successfully performed pars-plana vitrectomy and membrane peeling with two different types of dyes.