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.
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
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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