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Not Yet RecruitingNCT07418853

Comparison of Goniotomy Device Outcomes in Combined Phacoemulsification-goniotomy Surgeries

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
132 (estimated)
Sponsor
Henry Ford Health System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to determine of one of three different devices to perform goniotomy to treat glaucoma at the time of cataract surgery is more or less effective than the others. The primary outcomes are to compare intraocular pressure control and glaucoma medication use up to 6 months after surgery. Participants will under combined cataract surgery and goniotomy. They will have post-operative follow up visits at 1 day, 1 week, 1 month, 3 months, and 6 month

Conditions

Interventions

TypeNameDescription
PROCEDUREGoniotomyGoniotomy opens the trabecular meshwork to lower intraocular pressure.

Timeline

Start date
2026-03-01
Primary completion
2028-03-01
Completion
2028-03-01
First posted
2026-02-18
Last updated
2026-02-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07418853. Inclusion in this directory is not an endorsement.

Comparison of Goniotomy Device Outcomes in Combined Phacoemulsification-goniotomy Surgeries (NCT07418853) · Clinical Trials Directory