Clinical trial
A Multi-center Randomized Control Cross-over Study to Evaluate the Safety and…
NCT04908254 · Koya Medical, Inc., Industry · Completed
Key facts
| NCT number | NCT04908254 |
|---|---|
| Title | A Multi-center Randomized Control Cross-over Study to Evaluate the Safety and Effectiveness of the Dayspring Active Wearable Compression Device vs. an Advanced Pneumatic Compression Device for Treating Breast Cancer Related Lymphedema |
| Official title | A Multi-center Randomized Control Cross-over Study to Evaluate the Safety and Effectiveness of Dayspring Active Wearable Compression Device vs. an Advanced Pneumatic Compression Device for Treating Breast Cancer Related Lymphedema |
| Acronym | NILE |
| Lead sponsor | Koya Medical, Inc., Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Lymphedema, Lymphedema of Upper Arm, Breast Cancer |
| Intervention type | Device |
| Interventions | Crossover Device (PCD or Dayspring - alternate to first group) |
| Enrollment | 50 |
| Start date | Jun 1, 2021 |
| Primary completion | Dec 31, 2021 |
| Completion | Dec 31, 2021 |
| First posted | Jun 1, 2021 |
| Last update posted | Dec 9, 2025 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: