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NCT06289491 · ClinicalTrials.gov registry record · NA
A Trial of Hydrus Microstent Versus Goniotomy
A NA study of Glaucoma and Glaucoma Open-Angle, sponsored by Massachusetts Eye and Ear Infirmary.
- Recruiting
- Registry status
- NA
- Development phase
- 243
- Enrollment target
- 1
- Study location
NCT06289491 is a NA study of Glaucoma and Glaucoma Open-Angle that is actively recruiting participants, run by Massachusetts Eye and Ear Infirmary. The registered enrollment target is 243 participants, below the 908-participant average among 92 other Glaucoma trials with a reported enrollment target (73% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06289491, a NA study of Glaucoma and Glaucoma Open-Angle, is actively recruiting participants, sponsored by Massachusetts Eye and Ear Infirmary.
- RECRUITING
- Registry status
- NA
- Development phase
- 243 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to evaluate the comparative efficacy and safety of Hydrus Microstent, incisional goniotomy, and excisional goniotomy when combined with cataract surgery in patients with mild and moderate open-angle glaucoma. The main questions it aims to answer are: * How do the intraocular pressure lowering effects of these three microinvasive glaucoma surgeries compare? * How do the safety profiles of these three microinvasive glaucoma surgeries compare? Participants will be randomized to one of these three microinvasive glaucoma surgeries in combination with cataract surgery.
Conditions Studied
Interventions
- PROCEDURE Hydrus Microstent
- PROCEDURE Incisional goniotomy
- PROCEDURE Excisional goniotomy
Study Locations (1)
Massachusetts
- Massachusetts Eye and Ear - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 243 participants |
| Start Date | 2025-02-14 |
| Est. Completion | 2029-04 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06289491
The ClinicalTrials.gov registry entry for NCT06289491 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 243 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 908-participant average among 92 other Glaucoma trials with a reported enrollment target (73% lower). The listed sponsor is Massachusetts Eye and Ear Infirmary, which has 73 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Glaucoma appearing as the primary indexed condition, and to 3 interventions - of which Hydrus Microstent is the first listed.
NCT06289491 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT06289491 about?
NCT06289491 is a clinical study titled "A Trial of Hydrus Microstent Versus Goniotomy". The goal of this clinical trial is to evaluate the comparative efficacy and safety of Hydrus Microstent, incisional goniotomy, and excisional goniotomy when combined with cataract surgery in patients with mild and moderate open-angle glaucoma. The main questions it aims to answer are: * How do the ...
What is the current status of trial NCT06289491?
This trial is currently recruiting. It is a NA study. The enrollment target is 243 participants. The study started on 2025-02-14. Estimated completion is 2029-04.
What conditions does trial NCT06289491 study?
This clinical trial studies the following conditions: Glaucoma, Glaucoma Open-Angle.
What interventions are being tested in trial NCT06289491?
The interventions under investigation include: Hydrus Microstent (PROCEDURE), Incisional goniotomy (PROCEDURE), Excisional goniotomy (PROCEDURE).
Who is sponsoring clinical trial NCT06289491?
This trial is sponsored by Massachusetts Eye and Ear Infirmary, which has 73 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06289491 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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