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Clinical Trial Summary

The objective of this study is to assess the efficacy of the eXciteOSA device amongst a sample of patients with moderate OSA. The study is a multi-center, prospective, open-label, randomized, parallel-arm trial of eXciteOSA (administered at two doses) versus no-therapy for six weeks. Up to 120 participants will be enrolled, in order to randomized n=62.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05252156
Study type Interventional
Source Signifier Medical Technologies
Contact
Status Completed
Phase N/A
Start date March 21, 2022
Completion date October 31, 2022

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