A Study for Assessing the Safety of Hanita Glaucoma Shunt in Glaucoma Patients
NCT04796883 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16
Last updated 2022-03-02
Summary
The HANITA Glaucoma Filtration Device is intended to reduce intraocular pressure in glaucoma patients where medical and conventional surgical treatments have failed.
Conditions
Interventions
- DEVICE
-
Hanita Glaucoma shunt Ver.3.2
The procedure will be performed under anesthesia (at physician discretion) and a Hanita shunt devce will be implanted.
Sponsors & Collaborators
-
Hanita Lenses
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 40 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-06-30
- Primary Completion
- 2021-11-15
- Completion
- 2021-11-15
Countries
- Spain
Study Locations
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