NCT04897035

Study to Evaluate the Safety and Effectiveness of Dayspring for Lower Extremity Lymphedema

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

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 24 (actual)
• Sponsor: Koya Medical, Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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

Conditions

• Lymphedema
• Lymphedema Lower Extremity
• Chronic Venous Insufficiency
• Secondary Lymphedema

Interventions

Type	Name	Description
DEVICE	Dayspring Active Wearable Compression System	Dayspring Active Wearable Compression System

Timeline

• Start date: 2021-06-01
• Primary completion: 2022-06-30
• Completion: 2022-07-01
• First posted: 2021-05-21
• Last updated: 2026-02-17
• Results posted: 2026-01-29

Locations

2 sites across 1 country: United States

Regulatory

• FDA-regulated device study