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Clinical Trial Summary

This is a multicenter, prospective study designed to evaluate performance of the SVS in the REACH SVS control patients. The study is expected to enroll up to 20 patients at up to 12 sites with up to 6 patients per site.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02914340
Study type Interventional
Source Spiration, Inc.
Contact
Status Completed
Phase N/A
Start date September 2016
Completion date September 2018

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