Expired Study
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Fort Worth, Texas 76134


Purpose:

The purpose of the study is to compare femtosecond laser-assisted capsulotomy to manual capsulorhexis in patients with intumescent cataracts. An intumescent cataract is defined as a cataract with a pressurized capsular bag.


Criteria:

Inclusion Criteria: - Willing to undergo cataract surgery. - Able to lie flat in a supine position. - Able to understand and willing to sign the Informed Consent Form (ICF). - Presenting with intumescent white cataract, with a liquid pressurized bag and a milky, liquid cortex. - Other protocol-specified inclusion criteria may apply. Exclusion Criteria: - Pregnant or lactating mothers. - Corneal disease that precludes application of the cornea or transmission of laser light at 1030 nanometer (nm) wavelength. - Corneal opacity that would interfere with the laser beam. - Presence of blood or other material in the anterior chamber. - Hypotony or presence of corneal implant. - Poorly dilating pupils. - Condition which would cause inadequate clearance between the intended capsulotomy depth and the endothelium. - Residual, recurrent, active ocular or eye lid disease, including any corneal abnormality. - Any contraindication to cataract surgery. - Other protocol-specified exclusion criteria may apply.


NCT ID:

NCT02403206


Primary Contact:

Study Director
Clinical Manager, Surgical
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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