Expired Study
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Fort Worth, Texas 76134


Purpose:

The purpose of this study is to demonstrate that the Centurion® Vision System used with the 45° Balanced Tip will result in less Cumulative Dissipated Energy (CDE) than the lnfiniti® Vision System used with the 45° Mini-Flared Kelman (MFK) tip during cataract extraction surgery via phacoemulsification of cataract grades NII- NIV [Lens opacities classification system II (LOCSII)].


Criteria:

Inclusion Criteria: - Willing and able to consent for participation; - Willing and able to attend postoperative examinations per protocol schedule; - Cataract in at least one eye with a Nuclear Opalescence of II-IV (via LOCSII) followed by posterior chamber intraocular lens (IOL) implantation; - Other protocol-specified inclusion criteria may apply. Exclusion Criteria: - Planned multiple procedures, including Laser Phaco, LASIK, LRI's etc. during surgery or the course of this study; - Severe conditions of acute or chronic diseases or illnesses that would increase the operative risk or confound the result of this investigation; - Untreated or uncontrolled Glaucoma; - Previous intraocular or corneal surgery of any kind, including any type of surgery for either refractive or therapeutic purposes; - Poorly dilating pupil or other pupil defect; - Current or previous use of an alpha-1-selective adrenoceptor blocking agent or antagonist of alpha 1A adrenoceptor (eg, Flomax®, Hyntrin®, or Cardura®); - Severe retinal disorders; - Corneal disease or retinal detachment; - Other protocol-specified exclusion criteria may apply.


NCT ID:

NCT02502526


Primary Contact:

Study Director
Alcon, A Novartis Division
Alcon, A Novartis Division


Backup Contact:

N/A


Location Contact:

Fort Worth, Texas 76134
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 22, 2017

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