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Effective Phaco Time and Endothelial Cell Loss When Using Veritas

A

Aloha Vision Consultants

Status

Enrolling

Conditions

Cataract

Treatments

Device: Veritas Vision System

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT07176416
CY-25-01

Details and patient eligibility

About

This study is a single center, prospective study of cumulative dissipated energy and endothelial cells loss per phacoemulsification procedure after successful cataract surgery. Subjects will be assessed 3 months postoperatively at a single visit. Clinical evaluations will include central corneal thickness, specular microscopy, as well as measurement of visual acuities at distance.

Enrollment

50 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients undergoing age-related cataract surgery.
  • Planned use of the Catalys Precision Laser System.
  • Planned implantation of TECNIS intraocular lenses (IOLs).

Exclusion criteria

• Moderate-severe any disease state (deemed by the surgeon) that could increase risk of complicated cataract surgery (ie, pseudoexfoliation syndrome, zonular dehiscence, history of eye trauma, and prior refractive surgery).

Trial contacts and locations

1

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Central trial contact

Alana K Dunn

Data sourced from clinicaltrials.gov

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