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Cataract clinical trials

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NCT ID: NCT01019018 Completed - Cataract Clinical Trials

Efficacy of Subtenon's Block With Olive Tipped Cannula

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

The purpose of this study is to compare the efficacy of olive tip cannula to the standard Steven's cannula in performing subtenon's anesthesia for patients undergoing cataract surgery.

NCT ID: NCT01016405 Completed - Dry Eye Clinical Trials

Prospective Health Assessment of Cataract Patients' Ocular Surface

Start date: June 2009
Phase: N/A
Study type: Observational

This study will determine the incidence and severity of dry eye in patients undergoing cataract surgery as determined by grade on the International Task Force (ITF) scale.

NCT ID: NCT01014702 Active, not recruiting - Cataract Clinical Trials

Prospective Clinical Trial of the LensAR Laser System

Start date: November 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The LensAR Laser System is used to create an opening in the anterior capsule of the lens and fragments the cataractous lens. The study will evaluate clinical outcomes compared to the contra-lateral eye treated with conventional phacoemulsification surgery.

NCT ID: NCT01010490 Completed - Cataract Clinical Trials

Outcomes of Phacoemulsification With Torsional Ultrasound

Start date: May 2007
Phase: Phase 4
Study type: Interventional

To determine the differences in intra-operative complications, surgical duration, fluid usage, corneal thickness and endothelium cell density in eyes undergoing microcoaxial phacoemulsification (MCP) either with Torsional or longitudinal ultrasound during the surgery and at post-operative day 1, 1 month and 3 months.

NCT ID: NCT01001117 Active, not recruiting - Cataract Clinical Trials

Laser Treatment of the Crystalline Lens

Start date: October 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The use of a femtosecond laser in cataract surgery that gives equivalent or improved results comapred to conventional phaco-emulsification surgery.

NCT ID: NCT00999492 Completed - Cataracts Clinical Trials

Selection of Aspheric Diffractive Multifocal Intraocular Lens (IOLS) Based on Corneal Wavefront

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

Given the availability of aspheric diffractive IOLs with varying negative spherical aberration it may be feasible, by selecting the best fit IOL, to minimize aberrations and thereby maximize visual performance.

NCT ID: NCT00992355 Completed - Cataract Clinical Trials

Tobramycin-Dexamethasone Versus Tobramycin-Dexamethasone Plus Ketorolac After Phacoemulsification Surgery

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

This randomized controlled trial compares two regimens of topical therapy: - tobramycin 0.3% - dexamethasone 0.1% (TobraDex®, Alcon), one drop four times/day - combination of tobramycin 0.3% - dexamethasone 0.1% (TobraDex®, Alcon), one drop four times/day, plus Ketorolac tromethamine 0.5% (Acular®, Allergan), one drop three times/day. The topical treatment is administered for 28 days after phacoemulsification. Patients are independently assessed by two ophthalmologists. On day 28, patients are evaluated for - corneal edema - conjunctival redness - anterior chamber reaction. Moreover, the cases necessitating continuation of treatment are compared in the two groups on day 28 and 42.

NCT ID: NCT00986076 Completed - Inflammation Clinical Trials

Clinical Trial on Anti-inflammatory Effect of Low-Molecular Weight Heparin in Pediatric Cataract Surgery

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

The purpose of this study is to determine if intraocular infusion of low-molecular weight heparin (enoxaparin) influences postoperative inflammation following pediatric cataract surgery with intraocular lens (IOL) implantation.

NCT ID: NCT00974844 Completed - Cataract Clinical Trials

Posterior Assisted Levitation of Dropped Nucleus

PAL
Start date: January 2009
Phase: N/A
Study type: Observational

Dropping of nucleus is a common complication during cataract extraction by phacoemulsification. The investigators describe a new technique to retrieve the dropped nucleus by using an instrument called Pars Plana Levitator (ASICO-LLC, USA).

NCT ID: NCT00972621 Completed - Cataract Clinical Trials

Clinical Evaluation of a New Viscoelastic for Cataract Surgery

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

The purpose of this study is to evaluate the safety and effectiveness of a new opthalmic viscoelastic material for the use in cataract surgery. The new viscoelastic will be compared to a currently marketed viscoelastic material.