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Retinal Detachment clinical trials

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NCT ID: NCT01746875 Terminated - Clinical trials for Macular Degeneration

A Study Testing if Medicine Can Make Pigment Epithelium Detachments Regress and Stabilize the Vision in Eyes

Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine treatment effects in patients with retinal pigment epithelium detachment (PED) in relation to Age Related Maculopathy (AMD). Patients with newly diagnosed PED without choroidal neovascularisations (CNV), will be randomized to either treatment or observation. The treatment group will first be given injections with anti Vascular Endothelium Growth Factor (anti-VEGF). If the injections do not have any effect, Verteporfin Photodynamic Therapy (PDT) will be given. All patients will be followed for a period of 2 years. It is hypothesized that treatment stops the progression of the disease and stabilizes the vision in this subgroup of patients with AMD.

NCT ID: NCT01722656 Completed - Clinical trials for Submacular Vascularized Pigment Epithelial Detachments

Intravitreal Aflibercept Injection for the Treatment of Submacular Vascularized Pigment Epithelial Detachment

EVEN
Start date: November 2012
Phase: Phase 4
Study type: Interventional

This study will evaluate the use of intravitreal aflibercept (anti-VEGF therapy) in patients with a type of macular degeneration known as vascularized pigment epithelial detachment. Previous studies have shown a generally poor outcome in treating this difficult to treat form of wet macular degeneration. More recently, multiple pilot studies have shown positive benefits to using anti-VEGF therapy. This study will evaluate the safety and efficacy of treating vascularize pigment epithelial detachment associated with wet macular degeneration with intravitreal aflibercept injection.

NCT ID: NCT01716507 Completed - Retinal Detachment Clinical Trials

23 Gauge and 20 Gauge Vitrectomy for Rhegmatogenous Retinal Detachments

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

This study is a comparison (23 gauge vs 20 gauge instrumentation) of surgical instrumentation for retinal detachment repair.

NCT ID: NCT01670162 Active, not recruiting - Clinical trials for Age Related Macular Degeneration

On-label tReatment With Intravitreal Aflibercept injectiOn for Patients With Persistent Pigment epitheliaL Detachments in Neovascular Age Related Macular Degeneration (AMD)

ROLL
Start date: August 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of intravitreal aflibercept injection in a population of neovascular AMD patients that have been previously treated with 2.0 mg ranibizumab for persistent PEDs.

NCT ID: NCT01666236 Withdrawn - Clinical trials for Choroidal Neovascularization

Triple Treatment for Detachment of Retinal Pigment Epithelium Secondary to Polypoidal Choroidal Vasculopathy

Start date: September 2012
Phase: Phase 4
Study type: Interventional

Study the effectiveness of the treatment detachment of retinal pigment epithelium secondary to polypoidal choroidal vasculopathy. Efficacy will be assessed by regression of polyp area after twelve months, compared to baseline. Treatment under study is a triple therapy with: 1) reduced-fluence photodynamic therapy (PDT), 2) intravitreal (IVT) triamcinolone and, 3) IVT ranibizumab, for the treatment of detachment of the retinal pigment epithelium (PED) secondary to Polypoidal Choroidal Vasculopathy (PCV).

NCT ID: NCT01647373 Not yet recruiting - Clinical trials for Rhegmatogenous Retinal Detachment

Axial Length Change in Eyes Treated by Silicone Sponge Scleral Buckling

Start date: July 2013
Phase: N/A
Study type: Observational

All existing medical literatue regarding axial length (AL) changes after scleral buckling surgery for retinal detachment, descibes changes after solid silicone buckling. In this hospital, the investigators use only silicone sponge buckling, which has different properties and a different buckle profile. there are no studies in the literature describing tha AL changes after sponge buckling, or whether the AL change is less or more than with solid silicone buckles. The investigators wish to determine whether the AL change profile with their silicone sponge is significantly different, and if so, whether this is clinically important in determining the better choice of buckle material to be preferred.

NCT ID: NCT01639209 Completed - Clinical trials for Rhegmatogenous Retinal Detachment

Pneumatic Retinopexy Versus Vitrectomy for Retinal Detachment

Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this research study is to compare the outcomes of pneumatic retinopexy with the outcomes of vitrectomy (with or without scleral buckle) for the management of retinal detachment, in terms of anatomical success, functional success and impact on patient quality of life.

NCT ID: NCT01628354 Completed - Clinical trials for Choroidal Neovascularization

Study to Investigate the Safety and Efficacy of Ranibizumab in Patients With Choroidal Neovascularisation Due to Causes Other Than Age Related Macular Degeneration

Start date: February 2008
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that it is safe and effective to treat patients with choroidal neovascularisation (abnormal blood vessels growing under the retina) secondary to causes other than age related macular degeneration (AMD) and pigment epithelial detachments (blisters of fluid under the retina) secondary to AMD with ranibizumab (Lucentis). These groups of patients have to date been excluded from the multicentre trials demonstrating significant benefit of Ranibizumab in the treatment of AMD.

NCT ID: NCT01604616 Recruiting - Retinal Detachment Clinical Trials

Short Term Postoperative Tamponade Using Perfluorocarbon Liquid for Giant Retinal Tears

Start date: January 1998
Phase: N/A
Study type: Observational

The purpose of the article is, to investigate the efficacy and safety of perfluorocarbon liquid (PFCL) ,as a short term postoperative tamponade for treating retinal detachment ,associated with giant retinal tears.

NCT ID: NCT01589718 Withdrawn - Clinical trials for Proliferative Diabetic Retinopathy

A Study of the Safety, Tolerability, and Efficacy of IVT Pre-op 0.3mg Pegaptanib Sodium Versus Sham, for Management of Tractional Retinal Detachment and Vitreous Hemorrhage With Proliferative Diabetic Retinopathy

No-Crunch01
Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess whether preoperative pegaptanib sodium safely improves vitreous hemorrhage prior to surgical intervention and to evaluate the stability of pre-existing tractional retinal detachment.