Travoprost Implant with iStent for Open-Angle Glaucoma

Travoprost Intraocular Implant + iStent Infinite

Recruiting Phase 4 Interventional Study
Glaucoma, Open-Angle
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Glaukos Corporation · Industry
Who this trial is looking for

This trial is looking for adults with high eye pressure due to open-angle glaucoma or ocular hypertension. Participants will receive either a new treatment with an iStent or a sham procedure along with a travoprost implant, and they will be monitored for 12 months.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have open-angle glaucoma or high eye pressure.

You may not be able to join if

  • I have untreated eye pressure over 36 mmHg.
  • I am allergic to travoprost or its ingredients.
  • I have a vertical cup/disc ratio greater than 0.8 in my study eye.
  • I have vision worse than 20/80 in either eye.
  • I have any eye condition that may significantly affect my safety or the trial results.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * diagnosis of open-angle glaucoma or ocular hypertension * qualifying IOP in the study eye Exclusion Criteria: * unmedicated (washed out) IOP of \>36 mmHg in the study eye * hypersensitivity to travoprost or any other components of the travoprost intraocular implant * vertica…
Contacts

Study Director

949-739-8749

idoseclinical@glaukos.com

CONTACT

Study Manager

949-739-8749

idoseclinical@glaukos.com

CONTACT