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Implantable Device

Beacon Aqueous Microshunt for Glaucoma (Beacon Trial)

N/A
Waitlist Available
Research Sponsored by MicroOptx
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights

Beacon Trial Summary

This trial will test a new type of glaucoma surgery to see if it is safe and effective.

Beacon Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Effectiveness via Intraocular Pressure Reduction
Safety via Serious and Adverse Event Reporting
Secondary outcome measures
Kaplan-Meier Analysis of Failure
Mean Change from baseline in IOP
Number of topical IOP-lowering medications - Mean change from baseline
+4 more

Beacon Trial Design

1Treatment groups
Experimental Treatment
Group I: Beacon Aqueous MicroshuntExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

MicroOptxLead Sponsor
2 Previous Clinical Trials
18 Total Patients Enrolled
2 Trials studying Glaucoma
18 Patients Enrolled for Glaucoma

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Study of the Beacon Aqueous Microshunt in Patients With Refractory Glaucoma
2020. "Study of the Beacon Aqueous Microshunt in Patients With Refractory Glaucoma". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04072016.
~2 spots leftby Apr 2025
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