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Edema clinical trials

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NCT ID: NCT01946399 Terminated - Macular Edema Clinical Trials

Ozurdex Implant for Macular Edema After Treatment Failure With Anti-VEGF

Start date: September 2013
Phase: N/A
Study type: Interventional

To determine if Ozurdex implant can offer an effective treatment for macular edema associated with retinal vein occlusion when treatment with intravitreal Avastin, Lucentis, or Eylea have not demonstrated a significant response.

NCT ID: NCT01939691 Terminated - Macular Edema Clinical Trials

Macular Edema Nepafenac vs. Difluprednate Uveitis Trial

MEND
Start date: September 12, 2018
Phase: Phase 4
Study type: Interventional

Macular edema is a condition in which there is swelling in the macula, the part of the retina that gives you your best vision. This swelling can cause your vision to decline. When diagnosed early and treated, you vision usually can be preserved. However, if the swelling goes untreated for a long time, it can cause permanent vision loss. We think that the three eye drop regimens in this study, difluprednate, difluprednate plus nepafenac, and prednisolone acetate plus nepafenac, might be effective in treating uveitic macular edema. Patients who enter this study are randomized to one of the three regimens and followed for 24 weeks.

NCT ID: NCT01795209 Terminated - Macular Edema Clinical Trials

Ranibizumab for Macular Edema Secondary to Branch Retinal Vein Occlusion in Patients With Fair Vision

RVOFV
Start date: January 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of ranibizumab for the treatment of macular edema (ME) secondary to branch retinal vein occlusion (BRVO) in patients with initial fair visual acuity.

NCT ID: NCT01788475 Terminated - Clinical trials for Diabetic Macular Edema

Safety and Effectiveness of Ozurdex Steroid Implants for DME After Vitrectomy Surgery

Start date: February 22, 2013
Phase: N/A
Study type: Interventional

Currently medications injected intravitreally in previously vitrectomized eyes have a very short half-life due to enhanced clearance of the drug. The use of the Ozurdex (dexamethasone) implant may allow sustained levels of steroid delivery to patients with diabetic macular edema that have undergone prior vitrectomy. The sustained steroid levels may lead to improved central retinal thickness measurements and improved visual acuity.

NCT ID: NCT01471054 Terminated - Macular Edema Clinical Trials

Dexamethasone Intravitreal Implant for Treatment of Macular Edema After Plaque Radiotherapy of Uveal Melanoma

Start date: April 2014
Phase: Phase 2
Study type: Interventional

To evaluate the safety and efficacy of dexamethasone intravitreal implant (Ozurdex) and compare it with safety and efficacy of intravitreal bevacizumab in eyes with macular edema after plaque radiotherapy of uveal melanoma.

NCT ID: NCT01168258 Terminated - Clinical trials for Diabetic Retinopathy

Evaluation of Single Nucleotide Polymorphisms (SNPs) in Patients With and Without Diabetic Macular Edema

Start date: July 7, 2010
Phase: N/A
Study type: Observational

Background: - Diabetic macular edema (DME) is a common condition in people with diabetes. DME occurs when blood vessels in the eye leak fluid, resulting in swelling inside the back of the eye and progressive vision loss. Research has shown that good blood sugar control can reduce the risk and severity of DME. However, not all diabetic patients with poor blood sugar control develop DME, and some patients develop DME despite excellent blood sugar control. This suggests that other factors, such as genes or inherited traits, may predispose or protect a diabetic patient from developing DME. Objectives: - To investigate genetic factors that may influence the development of diabetic macular edema. Eligibility: - Individuals at least 18 years of age who have type 2 diabetes, with or without diabetic macular edema. Design: - The study will require one visit to the National Institutes of Health eye clinic. - Participants will be screened with a medical history and basic eye examination. Individuals who have certain eye diseases other than DME may not be allowed to enroll in the study. - Participants will provide a blood sample, and will receive fluorescein angiography (an injection of fluorescein dye, after which a camera will take pictures of the dye as it flows through the blood vessels in the eye). - No treatment will be provided as part of this protocol.

NCT ID: NCT01141881 Terminated - Clinical trials for Diabetic Macular Edema

Evaluation of the Role of Intravitreal Tissue Plasminogen Activator in Treatment of Refractory Diabetic Macular Edema

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

Purpose: to evaluate the effect of intravitreal injection of tissue plasminogen activator(tPA) in treatment of refractory diabetic macular edema(DME).

NCT ID: NCT01131585 Terminated - Clinical trials for Visual Impairment Due to Diabetic Macular Edema

Safety and Efficacy of Ranibizumab in Diabetic Macular Edema

RELATION
Start date: June 2010
Phase: Phase 3
Study type: Interventional

This study was designed to confirm the efficacy and safety of laser photocoagulation as adjunctive therapy to ranibizumab 0.5 mg versus laser monotherapy in patients with visual impairment due to Diabetic Macular Edema. A subgroup of patients with Proliferative Diabetic Retinopathy were included to evaluate the efficacy and safety of laser photocoagulation as adjunctive therapy to ranibizumab 0.5 mg versus laser monotherapy in this population.

NCT ID: NCT01118715 Terminated - Edema Clinical Trials

Use of Compression Glove to Prevent Complications After Distal Radius Fractures: a Randomized Controlled Trial

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

Distal radius fractures (DRF) are the most common type of fracture in the human body, and a large proportion of DRFs result in complications. Previously proposed preventive strategies have questionable efficacy and may impose additional risks on the patient. Because many complications secondary to distal radius fractures are associated with excessive swelling, a prophylactic means for edema reduction could dramatically reduce morbidity among this population. A compression glove is a non-invasive, non-pharmacological way to reduce edema. Previous studies have confirmed its utility in edema reduction after hand trauma and among patients with chronic inflammatory conditions, but none have sufficiently investigated the application to patients with distal radius fractures, a population in which this intervention could have a large impact. The investigators propose a randomized controlled trial to evaluate use of a compression glove during recovery among patients who have sustained an unstable distal radius fracture. The investigators hypothesize that patients who wear a compression glove after a distal radius fracture: - Will experience less edema - Will demonstrate greater functionality - Will recover more quickly - Will have lower incidence rates of carpal tunnel syndrome - Will have lower incidence rates of complex regional pain syndrome

NCT ID: NCT01042678 Terminated - Clinical trials for Diabetic Macular Edema

Study of MP0112 Intravitreal Injection in Patients With Diabetic Macular Edema

Start date: February 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the safety and tolerability of MP0112 (a novel, potentially long acting VEGF inhibitor) in patients with diabetic retinal edema.