iStent Inject New Enrollment Post-Approval Study
NCT04624698 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 358
Last updated 2024-02-23
Summary
Study to evaluate the rate of clinically relevant complications associated with iStent inject placement in the post-market setting.
Conditions
- Glaucoma, Open-Angle
- Glaucoma
Interventions
- DEVICE
-
iStent Inject Implantation
Subjects will be implanted with the iStent Injection Micro-Bypass device
Sponsors & Collaborators
-
Glaukos Corporation
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-09-22
- Primary Completion
- 2026-05-31
- Completion
- 2026-05-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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