Status:

COMPLETED

Clinical Evaluation of the Next Generation Phaco System

Lead Sponsor:

Johnson & Johnson Surgical Vision, Inc.

Conditions:

Cataract

Eligibility:

All Genders

22+ years

Phase:

NA

Brief Summary

This study is a prospective, open-label clinical study of the VERITAS Vision System. The study will be conducted at up to three sites, with minimum 55 eyes and up to 150 eyes to be treated. The inves...

Eligibility Criteria

Inclusion

  • Minimum 22 years of age.
  • Cataracts for which cataract extraction and posterior chamber IOL implantation have been planned.
  • Availability, willingness, ability and sufficient cognitive awareness to comply with study requirements, examination procedures, and visits.
  • Be willing to provide informed consent and authorization to disclose protected health information or equivalent documentation necessary to comply with applicable privacy laws pertaining to medical procedures in the governing countries.

Exclusion

  • Expected surgical difficulties at the time of cataract extraction, which may increase the potential for complications (e.g., persistent bleeding, significant iris damage, uncontrolled intraocular pressure change, or significant vitreous prolapse or loss).
  • Subjects with only one good eye (e.g. amblyopic condition etc.).
  • Subjects with conditions associated with increased risk of zonular rupture, including capsular or zonular abnormalities that may lead to IOL decentration, including pseudoexfoliation, trauma, or posterior capsule defects.
  • History or current use of alpha-1 antagonist medication (e.g., Flomax).
  • Any condition which, in the Investigator's opinion, would make it unsafe (for the subject or for the study personnel) to treat the subject as part of this research study or for which cataract surgery is contraindicated.
  • Pupil abnormalities (non-reactive, fixed pupils, or abnormally shaped pupils).
  • Is pregnant, or is breast feeding, or intend to become pregnant during the study.
  • Concurrent participation or expected participation in an interventional (i.e., surgical or pharmaceutical interventional) clinical trial within 14 days prior to study screening.

Key Trial Info

Start Date :

September 28 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2021

Estimated Enrollment :

79 Patients enrolled

Trial Details

Trial ID

NCT04332640

Start Date

September 28 2020

End Date

May 1 2021

Last Update

June 15 2022

Active Locations (2)

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Page 1 of 1 (2 locations)

1

ACE Eyecare, Inc

Bakersfield, California, United States, 93301

2

Grupo Oftalmo & Plastico, Centro de Oftalmologia y Cirugia Plastica

El Escalón, San Salvador Department, El Salvador