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Active clinical trials for "Cataract"

Results 381-390 of 1416

Nevanac 3-Month Safety Study With QID Dosing

Cataract

The purpose of this study is to determine the safety of Nevanac 0.1% compared to Acular LS 0.4% and Vehicle in patients treated before cataract surgery and for approximately 90 days following surgery.

Completed4 enrollment criteria

Accuracy of the Galilei Analyzer to Calculate the Effective Corneal Power After Corneal Refractive...

Cataracts

The purpose of this study is to determine the accuracy of the Galilei corneal analyzer to calculate the effective corneal power (keratometry, corneal curvature) in patients who have undergone both corneal refractive surgery and lens extraction with intraocular lens implantation.

Terminated10 enrollment criteria

Safety and Effectiveness of the Calhoun Vision Light Adjustable Intraocular Lens (LAL)

Cataracts

The primary objective of this study is to evaluate, for the visual correction of aphakia, the safety and effectiveness of the Calhoun Vision Light Adjustable intraocular lens (LAL) and Light Delivery Device (LDD) in treating postoperative residual refractive error by providing a stable, targeted refractive adjustment of the LAL power and lock-in treatments with the LDD.

Completed22 enrollment criteria

Age-Related Eye Disease Study (AREDS)

Macular DegenerationCataract1 more

To assess the clinical course, prognosis, and risk factors of age-related macular degeneration (AMD) and cataract. To evaluate, in randomized clinical trials, the effects of pharmacologic doses of (1) antioxidants and zinc on the progression of AMD and (2) antioxidants on the development and progression of lens opacities.

Completed1 enrollment criteria

Effect of Intraocular Lens (IOL) Centration and Tilt on Visual Performance With Clareon® Vivity®...

CataractLenses1 more

The goal of this observational study is to assess the effect of intraocular lens (IOL) movement in patients who have undergone Clareon® Vivity® IOL implantation. The main question it aims to answer is: Does an association exist between IOL movement and patient quality of vision? Participants implanted with Clareon® Vivity® and Vivity® Toric IOLs will be asked to do the following: consent to participate in the study allow researchers to access their personal medical records undergo a series of tests to assess the position of their IOLs and quality of vision Researchers will compare the patients' preoperative and postoperative test results to determine whether an association exists between IOL movement and patient quality of vision.

Not yet recruiting11 enrollment criteria

Safety and Efficacy of the Hydrophobic Intraocular Lens AsqelioTM Monofocal With Biaspheric Design...

CataractPseudophakia

The goal of this observational study is to learn about the Asqelio monofocal intraocular lens (IOL) model QLIO130C in patients undergoing cataract surgery. The aim of the study is to evaluate the lens implementation safety and efficacy after at least 24 months.

Not yet recruiting7 enrollment criteria

Tolerability and Toxicity of Topically Applied Nepafenac 0.3% vs Ketorolac 0.5%

Cataract

This study will examine the tolerability and toxicity of topically applied Nepafenac 0.3% vs ketorolac 0.5% among patients undergoing cataract surgery.

Completed16 enrollment criteria

OPEN-LABEL, MULTI-CENTER, PHASE 1b/2a CLINICAL TRIAL DESIGNED TO EVALUATE THE SAFETY AND EFFICACY...

Patients Having Undergone Unilateral Cataract Extraction and Implantation of a Monofocal

To evaluate the safety and efficacy of ocular iontophoresis with dexamethasone phosphate ophthalmic solution, EGP-437®, using the EyeGate® II Drug Delivery System (EGDS) in patients having undergone cataract surgery with implantation of a posterior chamber intraocular lens (IOL)

Completed5 enrollment criteria

Bausch & Lomb Ophthalmic Viscosurgical Device (OVD) Dispersive (DVisc40)

Cataract

A Study to Document the Safety and Effectiveness of a New OVD When Compared to a Control OVD

Completed8 enrollment criteria

A Randomized Study in Children Ages Birth Through Three Years Undergoing Unilateral Cataract Extraction...

Unilateral Cataract ExtractionCongenital Cataract

The purpose of this study is to evaluate the effect of OMS302 compared to phenylephrine when administered in irrigation solution during cataract extraction on intraoperative pupil diameter, acute postoperative pain, and safety in children birth through 3 years.

Completed24 enrollment criteria
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