Glaukos® iStent® Trabecular Micro-Bypass Stent System In Conjunction With Cataract Surgery Postmarket Registry

Glaukos

Status: Completed

Conditions: Primary Open-angle Glaucoma

Treatments: Device: iStent

Study type: Observational

Funder types: Industry

Identifiers

NCT01841437

GTS100-PAR

Details and patient eligibility

About

The purpose of this study is to observe the safety of the Glaukos® iStent® Trabecular Micro-Bypass Stent Model GTS100 in conjunction with cataract surgery in subjects with mild to moderate open-angle glaucoma.

Enrollment: 191 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Consecutive subjects in whom implantation of the iStent is attempted

Exclusion criteria

• Please refer to approved indications in Directions for Use

Trial design

191 participants in 1 patient group

iStent

Treatment:

Device: iStent