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Retinal Detachment clinical trials

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NCT ID: NCT00345007 Completed - Clinical trials for Rhegmatogenous Retinal Detachment

Macular Function After Scleral Buckle

Start date: June 2005
Phase: N/A
Study type: Observational

Assess recovery of macula function after successful scleral buckling surgery for rhegmatogenous retinal detachment by using the multifocal ERG in the postoperative period i.e. recovery of functional integrity 2. Assess the relationship between the neurosensory retina and the retinal pigment epithelium/choriocapillaris after scleral buckling i.e. recovery of structural integrity 3. Assess if there is a difference between macula function postoperatively, in eyes with retinal detachments involving the macula and those that do not.

NCT ID: NCT00279669 Completed - Clinical trials for Retinopathy of Prematurity

Ultrasound to Detect Evidence for Retinal Detachment in Retinopathy of Prematurity

Start date: December 2004
Phase:
Study type: Observational

Premature infants stand a risk of danger to the layer of the eye that creates sight that, if untreated, can cause severe vision problems, leading to blindness in some cases. This research study will use ultrasound to examine the eye for retinal changes of prematurity.

NCT ID: NCT00210067 Completed - Retinal Detachment Clinical Trials

A Study in Subjects With Retinal Detachment

Start date: May 2001
Phase: Phase 1
Study type: Interventional

The purpose of this trial is to access the tolerability of INS37217 Intravitreal Injection when administered intravitreally in subjects with macula-on or macula-off rhegmatogenous retinal detachment (RRD).

NCT ID: NCT00120445 Completed - Retinal Detachment Clinical Trials

Comparison of Air and Expansile Gas in Pneumatic Retinopexy

Start date: July 2004
Phase: Phase 3
Study type: Interventional

The objective of the study is to evaluate the results of using air versus expansile gas (perfluoropropane) in the treatment of rhegmatogenous retinal detachment by pneumatic retinopexy, comparing the retinal reattachment rate and post-operative visual recovery.

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.

NCT ID: NCT00000140 Completed - Retinal Detachment Clinical Trials

The Silicone Study

Start date: September 1985
Phase: Phase 3
Study type: Interventional

To compare, through a randomized, multicenter surgical trial, the postoperative tamponade effectiveness of intraocular silicone oil with that of an intraocular long-acting gas (initially sulfur hexafluoride [SF 6 ], later perfluoropropane [C 3 F 8 ]) for the management of retinal detachment complicated by proliferative vitreoretinopathy (PVR), using vitrectomy and associated techniques. To evaluate the ocular complications that result from the use of silicone oil and gas.