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Clinical Trial Summary

The study will evaluate the efficacy and safety of the implant and intra-ocular pressure (IOP) lowering effects with or without glaucoma medications. The procedure will be a stand-alone surgery. Overall, the patient will be asked to perform several examinations up to 24 months after surgery. The primary efficacy objective of the present study is to show the IOP reduction under medication 6 months after surgery compared to medicated diurnal IOP at screening.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03193736
Study type Interventional
Source iSTAR Medical
Contact
Status Completed
Phase N/A
Start date June 19, 2017
Completion date November 25, 2019

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