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A Clinical Study To Assess The Safety And Effectiveness Of The OMNI® Surgical System

Sponsored by Sight Sciences, Inc.

About this trial

Last updated 2 years ago

Study ID

07408

Status

Active, not recruiting

Type

Observational

Placebo

No

Accepting

18-75 Years
All
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 2 years ago

What is this trial about?

The purpose of this study is to evaluate the long-term safety and effectiveness of the OMNI® Surgical System in subjects who were treated under protocol #06213

What are the participation requirements?

Yes

Inclusion Criteria

No

Exclusion Criteria

- Systemic disease that, in the opinion of the Investigator, would put the subject's health at risk and/or prevent completion of required study visits

- Ocular pathology which, in the Investigator's judgment, would either place the subject at increased risk of complications, contraindicate washout, place the subject at risk of significant vision loss during the study period (e.g., wet age macular degeneration (AMD), corneal edema, Fuch's dystrophy, active intraocular infection or inflammation within 30 days prior to Screening Visit, etc.), or interfere with compliance to elements of the study protocol (e.g., returning to Investigator's office for follow-up visits)

Locations

Location

Status