Clinical Trials Logo

Vitreous Hemorrhage clinical trials

View clinical trials related to Vitreous Hemorrhage.

Filter by:

NCT ID: NCT00996437 Completed - Clinical trials for Proliferative Diabetic Retinopathy

Intravitreal Ranibizumab for Vitreous Hemorrhage Due to Proliferative Diabetic Retinopathy (N)

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

This study is being conducted to determine if intravitreal injections of ranibizumab decrease the proportion of eyes in which vitrectomy is performed compared with saline injections in eyes presenting with vitreous hemorrhage from proliferative diabetic retinopathy.

NCT ID: NCT00745498 Completed - Clinical trials for Proliferative Diabetic Retinopathy

Pre- and Intra-operative Intravitreal Bevacizumab Injection in Diabetic Vitrectomy

IBDV
Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of pre- and intra-operative bevacizumab injection on postoperative vitreous hemorrhage after diabetic vitrectomy.

NCT ID: NCT00596297 Completed - Clinical trials for Diabetic Retinopathy

Preoperative Bevacizumab for Vitreous Hemorrhage

IBEVI
Start date: November 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether preoperative intravitreal bevacizumab is effective in reducing intra-operative and postoperative bleeding in diabetic patients submitted to pars plana vitrectomy for vitreous hemorrhage.

NCT ID: NCT00411970 Completed - Clinical trials for Postoperative Complications

20- Versus 23- Gauge System for Pars Plana Vitrectomy

Start date: September 2004
Phase: Phase 4
Study type: Interventional

The aim of the present study is to compare the functional and clinical differences and advantages between a standard operating system and a newly developed even smaller system for pars plana vitrectomy. The present study may work out the possible advantages and disadvantages between the routinely used 20-gauge vitrectomy system and the newly developed 23-gauge device.

NCT ID: NCT00300014 Recruiting - Clinical trials for Recurrent Diabetic Vitreous Hemorrhage

Efficacy and Safety of Intravitreal Triamcinolone Acetonide in Eyes With Post Vitrectomy Diabetic Vitreous Hemorrhage

Start date: January 2006
Phase: N/A
Study type: Interventional

The Purpose of this study is compare the efficacy of intravitreal triamcinolone in clearing recurrent post-vitrectomy diabetic hemorrhage with conventional treatment, air-fluid exchange.

NCT ID: NCT00198510 Completed - Clinical trials for Diabetic Retinopathy

Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage

Start date: November 1998
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if intravitreal injection of Vitrase (ovine hyaluronidase) clears vitreous hemorrhage

NCT ID: NCT00198497 Completed - Clinical trials for Diabetic Retinopathy

Safety and Efficacy Study of Vitrase for Clearance of Severe Vitreous Hemorrhage

Start date: June 1999
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if intravitreal injection of Vitrase (ovine hyaluronidase) clears vitreous hemorrhage

NCT ID: NCT00155454 Completed - Diabetes Mellitus Clinical Trials

Intravitreal Long Acting Gas in the Prevention of Early Postoperative Vitreous Hemorrhage in Diabetic Vitrectomy

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

Recurrent vitreous hemorrhage after vitrectomy for complications of diabetic retinopathy is a common occurrence. The hemorrhage may appear within the first few weeks after surgery or months later. This complication may delay visual rehabilitation significantly and sometimes requires additional procedures or surgery, jeopardizing previous successful operation. The causes of bleeding are diverse. While evidence suggests fibrovascular proliferation from the sclerotomy sites or in the vitreous base may be an important source of recurrent vitreous hemorrhage, other origins of hemorrhage exist including lysed clot from residual vitreous skirt, injured retinal vessels from surgery, and incompletely removed fibrovascular tissues. The latter three conditions may be the major sources of early postoperative vitreous hemorrhage. We have shown that peripheral retinal cryotherapy along with cryo treatment at the sclerotomy sites may effectively reduce the incidence of fibrovascular proliferation at the inner surface of sclerotomy sites and prevent the late-onset recurrent vitreous hemorrhage. However, many patients still experience disturbing vitreous hemorrhage within the first two to three weeks after post-operative transient clear-up of the vitreous. We hypothesize that gas bubble within the vitreous cavity may mechanically temponade the fragile retinal vessels, and concentrate the coagulation factors in the vitreous cavity, allowing the integrity of vessel walls gradually recovers and thus preventing the occurrence of early postoperative recurrent vitreous hemorrhage. To test this hypothesis, a clinical study was undertaken to investigate the effect of long-acting gas infused into the vitreous cavity at the end of diabetic vitrectomy in the prevention of recurrent vitreous hemorrhage.

NCT ID: NCT00000162 Completed - Clinical trials for Macular Degeneration

Branch Vein Occlusion Study

Start date: July 1977
Phase: Phase 3
Study type: Interventional

To determine whether scatter argon laser photocoagulation can prevent the development of neovascularization. To determine whether peripheral scatter argon laser photocoagulation can prevent vitreous hemorrhage. To determine whether macular argon laser photocoagulation can improve visual acuity in eyes with macular edema reducing vision to 20/40 or worse.

NCT ID: NCT00000154 Completed - Clinical trials for Diabetic Retinopathy

Diabetic Retinopathy Vitrectomy Study (DRVS)

Start date: October 1976
Phase: Phase 3
Study type: Interventional

To compare two therapies, early vitrectomy and conventional management, for recent severe vitreous hemorrhage secondary to diabetic retinopathy. Conventional management includes vitrectomy if hemorrhage fails to clear during a waiting period of 6 to 12 months or if retinal detachment involving the center of the macula develops at any time. To compare early vitrectomy and conventional management in eyes that have good vision but a poor prognosis because they are threatened with hemorrhage or retinal detachment from very severe proliferative retinopathy. To study the natural history of severe proliferative diabetic retinopathy.