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Cataract clinical trials

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NCT ID: NCT00690222 Terminated - Cataract Clinical Trials

Intracameral Mydriasis Versus Topical Mydriasis in Cataract Surgery

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

The purpose is to determine if an intracameral solution of 0.2% tropicamide and 2% phenylephrine can dilate the pupil for cataract surgery as well as pre-operative topical 1% tropicamide and 5% phenylephrine. We will be looking at two separate groups of patients, those with and those without pseudoexfoliation syndrome. We will be looking at how each method affects the size of the pupil at the beginning and at the end of cataract surgery. In addittion, we will look at what effect the two different methods have on blood pressure and heart rate in the pre-operative, peri-operative and post-operative periods.

NCT ID: NCT00596492 Terminated - Mature Cataracts Clinical Trials

DY002: Safety and Effectiveness of DYME as an Agent for Selective Staining of the Anterior Capsule During Cataract Surgery

AQNA-DY002
Start date: May 2008
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to test the hypothesis that DYME is safe and effective as a drug to facilitate continuous curvilinear capsulorhexis (CCC) by selectively staining the anterior capsule. Secondary objectives are to compare the safety and effectiveness of DYME to that of a smaller dose of the same API.

NCT ID: NCT00431028 Terminated - Inflammation Clinical Trials

Sub-Tenon's Injection of Triamcinolone and Ciprofloxacin in a Controlled-Release System for Cataract Surgery

Start date: September 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to compare one intraoperative sub-Tenon's capsule injection of triamcinolone and ciprofloxacin in a biodegradable controlled-release system with conventional prednisolone and ciprofloxacin eye drops to treat ocular inflammation and for infection prophylaxis after cataract surgery.

NCT ID: NCT00425464 Terminated - Cataract Clinical Trials

A Prospective Multicenter Clinical Study to Evaluate the Safety and Effectiveness of the Synchrony Dual Optic Intraocular Lens in Patients Undergoing Cataract Extraction

Start date: November 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if the Synchrony Dual Optic Accommodating Intraocular Lens can be used safely and effectively in post cataract extraction subjects

NCT ID: NCT00000157 Terminated - Cataract Clinical Trials

Randomized Trial of Aspirin and Cataracts in U.S. Physicians

Start date: April 1982
Phase: Phase 3
Study type: Interventional

To determine whether 325 mg of aspirin taken on -alternate days reduces the risk of developing cataract among male U.S. physicians who were aged 40 to 84 in 1982. To identify potential risk factors for cataract development, such as age, blood pressure, blood cholesterol, height, diabetes, medication use, and history of previous eye trauma or surgery.