Compression; Vein Clinical Trial
Official title:
Safety and Feasibility of the ElastiMed's SACS - Smart Active Compression Stocking
The main objective of this study is to demonstrate the safety and the feasibility of this
device, and its ability to increase venous blood flow
Primary safety Endpoint:
To demonstrate the safety of the device- no serious adverse effect
Primary feasibility Endpoint:
Increase the blood flow velocity
The blood flow will be detected by a Duplex Ultrasonography test at the popliteal vein and
the femoral vein.
The volunteers will rest at controlled environment room . Measurements will be performed
after 30 min of rest without the device on the leg (baseline) and after 30 min of device
activity .
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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| Terminated |
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| Completed |
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Phase 1 |