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Clinical Trial Summary

This is a prospective, multi-site, safety and feasibility study of the SalutarisMD SMD-DA system for retrobulbar minimally invasive episcleral brachytherapy device in patients receiving and not responding to anti-VEGF therapy for nAMD. The trial will be open label and non-randomized. The study intervention is a one-time intervention and requires no alteration to the standard of care during the follow-up period.


Clinical Trial Description

Subjects will receive a single brachytherapy treatment and 36 months of follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02988895
Study type Interventional
Source Salutaris Medical Devices, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date August 1, 2017
Completion date May 2025