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Clinical Trial Summary

An interventional, open, prospective, multi-center pre-market clinical investigation according to §§20-23a Medizinproduktegesetz (MPG, medical devices act), in which a total of 40 eyes of 40 consecutive patients at up to five (5) clinical sites will be enrolled, treated with the VISULAS green with option CSLT, and followed for a three months period. The primary objective of this clinical investigation is to evaluate safety and effectiveness of SLT with the VISULAS green laser with option CSLT.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04519814
Study type Interventional
Source Carl Zeiss Meditec AG
Contact
Status Active, not recruiting
Phase N/A
Start date June 3, 2020
Completion date October 2022

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