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Trabecular Micro-Bypass Stent

iStent for Glaucoma

N/A
Waitlist Available
Research Sponsored by Glaukos Corporation
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 36 months
Awards & highlights

Study Summary

The purpose of this study is to assess the long-term safety of the Glaukos® iStent® Trabecular Micro-Bypass Stent Model GTS100 in conjunction with cataract surgery vs. cataract surgery only, in subjects with mild to moderate open-angle glaucoma.

Eligible Conditions
  • Glaucoma

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~36 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 36 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
Rate of sight-threatening adverse events
Secondary outcome measures
Other adverse events
Other outcome measures
Diurnal IOP reduction ≥ 20%

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: iStentExperimental Treatment1 Intervention
Implantation of one iStent in conjunction with cataract surgery
Group II: Cataract surgeryActive Control1 Intervention
Cataract surgery alone
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
iStent
2009
Completed Phase 4
~1020

Find a Location

Who is running the clinical trial?

Glaukos CorporationLead Sponsor
65 Previous Clinical Trials
8,680 Total Patients Enrolled
35 Trials studying Glaucoma
4,614 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.
~31 spots leftby Apr 2025