Trials / Completed
CompletedNCT03330925
Safety and Feasibility of the ElastiMed's SACS
Safety and Feasibility of the ElastiMed's SACS - Smart Active Compression Stocking
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 11 (actual)
- Sponsor
- ElastiMed ltd · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
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 .
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ElastiMed's SACS | A wearable medical device that improve circulation using smart materials |
Timeline
- Start date
- 2018-01-24
- Primary completion
- 2018-12-03
- Completion
- 2018-12-03
- First posted
- 2017-11-06
- Last updated
- 2019-06-06
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT03330925. Inclusion in this directory is not an endorsement.