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A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Dayspring Active Wearable Compression Technology for Treating Lower Extremity Lymphedema — TIBER  

Lymphedema Clinical Trial

Official title:
A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Dayspring Active Wearable Compression Technology for Treating Lower Extremity Lymphedema

Clinical Trial Summary

A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Koya Dayspring Active Wearable Compression Technology for Treating Lower Extremity Lymphedema

Clinical Trial Description

A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Koya Dayspring Active Wearable Compression Technology for Treating Lower Extremity Lymphedema ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04897035
Study type Interventional
Source Koya Medical, Inc.
Contact
Status Completed
Phase N/A
Start date June 1, 2021
Completion date July 1, 2022
View Details
See also
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