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Cataract clinical trials

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NCT ID: NCT03587909 Completed - Cataract Surgery Clinical Trials

FLACS vs Phaco in Shallow Anterior Chamber

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Phacoemulsification in eyes with a shallow anterior chamber (ACD < 2.2mm) presents with problems of safe access to the cataract and increased vulnerability of the endothelium and a higher tendency of complications such as descemet's detachment and iris prolapse. A shallow anterior chamber is also responsible for the high incidence of glaucoma and postoperative complications after cataract surgery. Femtosecond assisted cataract surgery has made cataract surgery safer and more predictable. The effective phacoemulsification time and intra-operative manipulation is greatly reduced in FLACS. However phacoemulsification still remains the most widely performed cataract surgery around the world. Post-operative outcomes after phacoemulsification in patients having shallow anterior chamber have been extensively reported in literature over the years. There is no head to head comparison in terms of intraoperative performance and post-operative outcomes between FLACS and phacoemulsification in eyes with shallow anterior chamber. The aim is to compare the intra-operative performance and post-operative outcomes in eyes undergoing femtosecond laser assisted cataract surgery versus eyes undergoing phacoemulsification in eyes having shallow anterior chamber. The study will bring an understanding on the question: Do patients undergoing Femtosecond laser assisted cataract surgery behave differently from those undergoing phacoemulsification?

NCT ID: NCT03584139 Completed - Cataract Clinical Trials

IRIS Hook Assisted Phacoemulsification in Vitrectomized Eyes

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

Although phacoemulsification in previously vitrectomized eyes is a relatively safe procedure comparing with extracapsular cataract surgery, it is still more challenging than in eyes without previous vitrectomy because of the anatomical differences after PPV. Intraoperative difficulties such as abnormal anterior chamber deepening, unstable posterior capsules, and weakened zonules have been reported. The investigators aim to evaluate the efficacy and safety of a new simple iris hook assisted maneuver in phacoemulsification, then compare the incidence of intraoperative and postoperative complications of this technique with traditional phacoemulsification and phacoemulsification with 25-gauge vitreous irrigation. The latter two surgery methods are currently popular for cataract in vitrectomized eyes.

NCT ID: NCT03580473 Completed - Cataract Clinical Trials

Efficacy and Safety of Saturno IIB Association on the Control of Ocular Inflammation Post-phacoemulsification

Start date: February 27, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of Saturno II association on the control of ocular inflammation post-phacoemulsification

NCT ID: NCT03579433 Completed - Cataract Clinical Trials

Postmarket Study of an Intraocular Lens Power Selection System

Start date: August 16, 2018
Phase: N/A
Study type: Interventional

The purpose of the study was to evaluate the visual acuity outcomes when using the Optiwave Refractive Analysis (ORA) with VerifEye+ and Barrett Toric Calculator for calculating intraocular lens (IOL) power and axis in subjects requiring cataract surgery and implanted with a toric IOL in both eyes.

NCT ID: NCT03578276 Completed - Cataract Clinical Trials

Prophylactic Treatment: Lessdrops™ vs Standard Drops Regimen

Start date: June 22, 2018
Phase: Phase 4
Study type: Interventional

To compare the use of a compounded eye drop containing an antibiotic, a non-steroidal and steroidal anti-inflammatory to standard of care that is the use of 3 different topical medications to prevent inflammation and infection after routine cataract surgery.

NCT ID: NCT03531697 Completed - Clinical trials for Inflammation Following Ocular Surgery

Study of Loteprednol Etabonate in Adults Undergoing Bilateral Cataract Surgery

Start date: April 26, 2018
Phase: Phase 1
Study type: Interventional

This study will assess the bioequivalence of Loteprednol Etabonate and the reference listed drug (RLD)

NCT ID: NCT03531671 Completed - Cataract Clinical Trials

Assessing the Optics of the Eye Pre- and Post-operatively in Cataract

CAT
Start date: August 30, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate if a novel instrument called a Binocular Optical Coherence Tomographer (OCT) may resolve many of the issues with the assessment of patients with cataract.

NCT ID: NCT03512626 Completed - Cataract Senile Clinical Trials

Clinical Evaluation of Multifocal Intraocular Lens: OPTIVIS.TM

MFIOL
Start date: June 4, 2014
Phase: N/A
Study type: Interventional

This study evaluated visual outcome after cataract surgery with bilateral implantation of either a diffractive - refractive (hybrid) multifocal intraocular lens (MFIOL) or monofocal intraocular lens (IOL) as a control grup.

NCT ID: NCT03511638 Completed - Cataract Clinical Trials

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

Start date: May 9, 2018
Phase: N/A
Study type: Interventional

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

NCT ID: NCT03508778 Completed - Cataract Clinical Trials

Clinical Evaluation of the FluidVision Accommodation Intraocular Lens (AIOL)

CLEAR
Start date: February 27, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the safety and effectiveness of an investigational IOL in providing a range of vision as compared to a commercially available trifocal IOL in subjects undergoing cataract extraction and IOL implantation.