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Clinical Trial Summary

In this study, the investigators want to investigate the success of aqueous humor shunting in the retrobulbar space, using the eyeTube in combination with the eyeWatch implant. The investigators postulate that posterior aqueous humor shunting would be more effective, as this space offers a larger drainage area and a less aggressive local inflammatory environment than the subconjunctival space close to the limbus, resulting in lower and better-sustained IOP than in the more limited, fibroblast-promoting subconjunctival environment surrounding standard implants.


Clinical Trial Description

n/a


Study Design


NCT number NCT05912790
Study type Interventional
Source Rheon Medical SA
Contact
Status Active, not recruiting
Phase N/A
Start date June 6, 2023
Completion date September 30, 2024