iStent Inject New Enrollment Post-Approval Study

  • End date
    May 24, 2026
  • participants needed
  • sponsor
    Glaukos Corporation
Updated on 24 April 2022


Study to evaluate the rate of clinically relevant complications associated with iStent inject placement in the post-market setting.


To evaluate the rate of clinically relevant complications associated with iStent inject placement and stability, as determined at 36 months in the postmarket setting.

Condition Glaucoma, Open-Angle, Glaucoma
Treatment iStent Inject Implantation
Clinical Study IdentifierNCT04624698
SponsorGlaukos Corporation
Last Modified on24 April 2022


Yes No Not Sure

Inclusion Criteria

Male or female ≥ 22 years of age
Mild to moderate primary open-angle glaucoma
Scheduled to undergo cataract surgery
Able and willing to attend scheduled follow-up exams for three years postoperatively
Able and willing to provide written informed consent on the IRB approved Informed Consent Form
Operative Inclusion Criterion
Successful, uncomplicated cataract surgery

Exclusion Criteria

Angle closure glaucoma
Traumatic, malignant, uveitic, or neovascular glaucoma or discernible congenital anomalies of the anterior chamber angle
Retrobulbar tumor, thyroid eye disease, Sturge-Weber Syndrome or any other type of condition that may cause elevated episcleral venous pressure
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact



Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider


Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 



Reply by • Private

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note