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NCT05868772 | COMPLETED | Cataract

What is the Efficiency When Comparing Active Sentry at Low IOP vs Ozil at High IOP?
Sponsor:

Cataract and Laser Institute of Southern Oregon

Brief Summary:

The objective is to assess the efficiency of the Active Sentry handpiece at low intraocular pressure (IOP) compared with the Ozil at high IOP.

Condition or disease

Cataract

Intervention/treatment

Active Sentry Handpiece

Ozil Handpiece

Detailed Description:

This study is a single site, single-masked, randomized, prospective, contralateral eye study of the efficiency of the Active Sentry handpiece at low IOP compared with the Ozil at high IOP.

Study Type : OBSERVATIONAL
Estimated Enrollment : 36 participants
Official Title : What is the Efficiency When Comparing Active Sentry at Low IOP vs Ozil at High IOP?
Actual Study Start Date : 2023-05-16
Estimated Primary Completion Date : 2024-04-19
Estimated Study Completion Date : 2024-04-19

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 50 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: 1
Criteria
Inclusion Criteria
  • Subjects are eligible for the study if they meet the following criteria
    • Note: Ocular criteria must be met in both eyes.
    • * Be eligible to undergo sequential bilateral uncomplicated cataract surgery.
    • * Undergo uneventful cataract surgery.
    • * Gender: Males and Females.
    • * Both eyes must have same grade of cataract.
    • * Willing and able to provide written informed consent for participation in the study.
    • * Willing and able to comply with scheduled visits and other study procedures.
    Exclusion Criteria
    • If any of the following exclusion criteria are applicable to the subject or either eye, the subject should not be enrolled in the study.
    • * Patient under 50 years of age.
    • * Unable to complete sequential bilateral cataract surgery in both eyes by the same surgeon (JS).
    • * Patient cataract surgery complicated by posterior capsular tear.
    • * Any disease state deemed by PI that increases risk of complicated cataract surgery (ie Pseudoexfoliation syndrome, zonular dehiscence, history of eye trauma, RA, prior refractive surgery, etc).
    • The principal investigator reserves the right to declare a patient ineligible or non-evaluable based on medical evidence that indicates they are unsuitable for the trial.
    • Pregnancy has a known effect on the stability of refractions and visual acuity. As such, subjects who become pregnant during the study will not be discontinued but their data may be excluded from analyses of effectiveness.
What is the Efficiency When Comparing Active Sentry at Low IOP vs Ozil at High IOP?

Location Details

NCT05868772

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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

Not yet recruiting

United States, Oregon

Cataract & Laser Institute

Medford, Oregon, United States, 97504