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Clinical Trial Summary

To measure the efficacy and safety outcomes of SLT performed by optometrists.


Clinical Trial Description

Participants will undergo a pre-procedure examination in order to record baseline findings and to determine if they meet the inclusion criteria in order to undergo the procedure. Participants will undergo the SLT procedure and will be examined at 1 hour, 1 week and 6 weeks. Follow up examinations will evaluate eye pressure reduction and post-procedure complications. The rate complication post-procedure are typically low. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04036214
Study type Observational
Source Northeastern State University
Contact
Status Active, not recruiting
Phase
Start date August 21, 2019
Completion date August 30, 2022

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