Trials / Not Yet Recruiting
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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Goniotomy | Goniotomy 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.