ClinicalTrials.gg
RecruitingNCT06066645Updated Jun 2, 2026

Travoprost Intraocular Implant + iStent Infinite

A Phase 4 interventional study of Travoprost Intraocular Implant and iStent infinite in Glaucoma, Open-Angle, sponsored by Glaukos Corporation. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-02.

Sponsored by Glaukos Corporation · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2023; still recruiting 3 years 1 month later.
Phase
Phase 4
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Adult subjects with elevated intraocular pressure will be randomized to receive iStent infinite trabecular bypass system plus a travoprost intraocular implant or receive a sham procedure plus a travoprost intraocular implant and be followed for 12 months.

02

Conditions studied

  • Glaucoma, Open-Angle

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03

In context

Glaucoma, Open-Angle

924 studies on the registry are indexed under Glaucoma, Open-Angle; 117 are open to participants now.

This study's planned enrollment of 150 is above the median of 80 across 692 interventional studies indexed under Glaucoma, Open-Angle.

Browse Glaucoma, Open-Angle studies →

Lead sponsor

Glaukos Corporation is the lead sponsor of 67 studies on the registry; 14 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 7 (54%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • diagnosis of open-angle glaucoma or ocular hypertension
  • qualifying IOP in the study eye

Exclusion criteria

Exclusion Criteria:

  • unmedicated (washed out) IOP of >36 mmHg in the study eye
  • to travoprost or any other components of the travoprost intraocular implant
  • vertical cup/disc ratio > 0.8 in the study eye
  • best spectacle corrected visual acuity of worse than 20/80 in either eye
  • any ocular disease or condition that, in the opinion of the investigator, may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
150 participants (estimated)

Study arms

  • Experimental
    iDose TR

    Travoprost Intraocular Implant in subjects who had successful iStent infinite placement

    Drug: Travoprost Intraocular Implant · Device: iStent infinite

  • Active comparator
    iDose TR alone

    Travoprost Intraocular Implant

    Drug: Travoprost Intraocular Implant · Other: Sham procedure

Interventions

  • anchored intracameral implant containing travoprost

    Also known as: iDose TR

  • DeviceiStent infinite

    Successful iStent infinite surgery

  • OtherSham procedure

    Sham procedure (to mimic placement of an iStent infinite)

06

What researchers measure

Primary outcomes

  1. change from baseline in mean diurnal intraocular pressure (IOP)

    mean diurnal IOP at the 3 month visit minus mean diurnal IOP at baseline

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
  • Glaukos Clinical Study Site
    Oklahoma City, Oklahoma 73112, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06066645
Responsible party
Sponsor
First posted
Oct 4, 2023
Start date
Sep 14, 2023
Primary completion
May 2027 (estimated)
Completion
Feb 2028 (estimated)
Last update
Jun 2, 2026

Study contacts

Study Director
Contact
idoseclinical@glaukos.com
949-739-8749
Study Manager
Contact
idoseclinical@glaukos.com
949-739-8749
Study Director
study director · Glaukos Corporation

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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