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NCT07418853 · ClinicalTrials.gov registry record · NA

Comparison of Goniotomy Device Outcomes in Combined Phacoemulsification-goniotomy Surgeries

A NA study, sponsored by Henry Ford Health System.

Not yet
Registry status
NA
Development phase
132
Enrollment target

NCT07418853 is a NA study that has not yet begun recruiting, run by Henry Ford Health System. The registered enrollment target is 132 participants.

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The verdict

NCT07418853, a NA study, has not yet begun recruiting, sponsored by Henry Ford Health System.

NOT YET RECRUITING
Registry status
NA
Development phase
132 participants
Enrollment target

Study 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

Interventions

  • PROCEDURE Goniotomy

Trial Details

FieldValue
Enrollment Target 132 participants
Start Date 2026-07-01
Est. Completion 2028-03-01
Phase NA

Sponsor

Henry Ford Health System

234 total trials

What the Registry Record Tells You About NCT07418853

The ClinicalTrials.gov registry entry for NCT07418853 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 132 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Goniotomy is the first listed.

NCT07418853 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07418853 about?

NCT07418853 is a clinical study titled "Comparison of Goniotomy Device Outcomes in Combined Phacoemulsification-goniotomy Surgeries". 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...

What is the current status of trial NCT07418853?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 132 participants. The study started on 2026-07-01. Estimated completion is 2028-03-01.

What interventions are being tested in trial NCT07418853?

The interventions under investigation include: Goniotomy (PROCEDURE).

Who is sponsoring clinical trial NCT07418853?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.