Safety and Feasibility of the ElastiMed's SACS

Compression; Vein Clinical Trial

Official title:
Safety and Feasibility of the ElastiMed's SACS - Smart Active Compression Stocking

Status Completed

Clinical Trial 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 .

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Compression; Vein

Clinical Trial Details

NCT number	NCT03330925
Study type	Interventional
Source	ElastiMed ltd
Contact
Status	Completed
Phase	N/A
Start date	January 24, 2018
Completion date	December 3, 2018

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT04096729` - Patients Commitment to Compression Therapy
Not yet recruiting	`NCT06438133` - Digital Supported Compression Bandaging in Patients With Chronic Edema in the Lower Limbs
Terminated	`NCT05212363` - Lower Leg Compression in Extended Video Game Play: A Pilot Study	N/A
Completed	`NCT03725111` - Haemodynamics Variations of Transcutaneous Oxygen in Patient With Areterio-venous Leg Ulcers Under Venous Compression	N/A
Recruiting	`NCT04837560` - Safety and Efficacy of the ElastiMed's SACS 2.0 - Smart Active Compression Stocking for the Treatment of Venous Edema	Phase 1