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A Prospective Evaluation of Open-Angle Glaucoma Subjects on Two Topical Hypotensive Medications Treated With One Suprachoroidal Stent

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Glaukos

Status and phase

Completed
Phase 4

Conditions

Subject With Primary Open-angle Glaucoma (POAG)

Treatments

Device: iStent Supra Stent

Study type

Interventional

Funder types

Industry

Identifiers

NCT01252914
GCF-019

Details and patient eligibility

About

The purpose of this study is to assess the efficacy and safety of one iStent supra stent in the reduction of intraocular pressure associated with primary open-angle glaucoma.

Full description

The study assesses the efficacy and safety of one iStent supra stent in the reduction of intraocular pressure associated with primary open-angle glaucoma.

Enrollment

80 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Diagnosed with primary open-angle glaucoma (POAG)
  • Subjects on two topical hypotensive medications

Exclusion criteria

  • Traumatic, uveitic, neovascular, or angle closure glaucoma
  • Fellow eye already enrolled

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

One iStent Supra Stent and medication
Experimental group
Description:
The study assesses the efficacy and safety of one iStent Supra stent in the reduction of intraocular pressure associated with primary open-angle glaucoma
Treatment:
Device: iStent Supra Stent

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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