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Glaukos® iStent Infinite Trabecular Micro-Bypass System in Subjects With Mild to Moderate Primary Open-angle Glaucoma

Glaukos Corporation · NCT06057051

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 35+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Not applicable
Target enrollment
245
US sites recruiting
1
Study start
September 1, 2023
Record last updated
September 28, 2023

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

Prospective, multicenter, single-arm study of the iStent infinite in adult pseudophakic or phakic subjects with mild to moderate primary open angle glaucoma who have not failed conventional medical and surgical treatment

Being studied: iStent Infinite

Conditions: Glaucoma

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Diagnosis of primary open-angle glaucoma
  • Phakic or pseudophakic
  • Age 35 years or older

Exclusion Criteria

  • Traumatic, uveitic, neovascular, angle-closure glaucoma or
  • glaucoma associated with vascular disorders
  • Active corneal inflammation or edema
  • Retinal disorders not associated with glaucoma

Recruiting US locations

  • Glaukos Investigator Site

    Cincinnati, OH 45242

    Site contact: Dari Parizadeh

Study contacts (from the official record)

  • Dari Parizadeh · 949-481-0575 · dparizadeh@glaukos.com
  • Kerry Stephens · 949-481-8057 · kstephens@glaukos.com
Glaukos® iStent Infinite Trabecular Micro-Bypass System in… (NCT06057051) | Bored Studies