Feasibility Clinical Evaluation of the Calibreye System
NCT05885022 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2025-12-15
Summary
To evaluate the safety and feasibility of the Calibreye System in patients with open angle glaucoma.
Conditions
- Glaucoma, Open-Angle
Interventions
- DEVICE
-
Calibreye System
Implantation of a glaucoma device to reduce intraocular pressure
Sponsors & Collaborators
-
Myra Vision Inc.
lead INDUSTRY
Principal Investigators
-
Keith Barton, MD · Moorfields Eye Hospital NHS Foundation Trust
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-05-31
- Primary Completion
- 2027-12-31
- Completion
- 2028-12-31
- FDA Device
- Yes
Countries
- India
- Mexico
- Panama
Study Locations
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