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COMPLETEDNANCT00366665

Comparison of the Performance of the Infiniti Vision and the Series 20000 Legacy Phacoemulsification Systems

To compare the efficiency of the Infiniti vision system and the Series 20000 Legacy System phacoemulsification units during routine cataract extraction.

Lead sponsor: Medical University of South Carolina•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Medical University of South Carolina

Age

50 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Cataract
•Eligible for cataract extraction with primary implantation of a posterior chamber IOL
•2 to 3+ cataract density

Exclusion Criteria

•Preoperative ocular pathology that can affect visual acuity
•Corneal irregularities such as keratoconus, corneal dystrophy, corneal opacities.
•Previous intraocular or corneal surgery.
•Other ocular surgery at the time of the cataract extraction.
•Significant intraoperative intraocular bleeding
•Detached Descemet's membrane
•Implantation of the intraocular lens in the anterior chamber or sulcus

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: August 21, 2006Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment30

Start dateMar 2005

Last updatedAug 21, 2006

Condition

Cataract Extraction

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: August 21, 2006Data synced to Clareo: June 27, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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