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Neuromuscular Stimulation Versus Intermittent Compression for Venous Thromboembolism Prophylaxis in Critical Care — ENSARIA  

Sepsis Clinical Trial

Official title:
Electronic Neuromuscular Stimulation Versus Intermittent pneumAtic Compression Devices for the pRevention of Venous Thromboembolic Disease in Critically Ill Adults: a Randomised Feasibility Study

Clinical Trial Summary

In this prospective, randomised, open-label, parallel group, feasibility trial; the investigators will objectively assess whether it is feasible to apply the Geko device to critically ill adults for the prevention of venous thromboembolism (VTE) compared to usual care with intermittent pneumatic compression devices (IPCs).

Clinical Trial Description

VTE is a common problem amongst patients in critical care. Current measures include intermittent pneumatic compression devices, used to aid the venous return of blood from the lower limbs. These devices are contraindicated and/or poorly tolerated by some patients. Neuromuscular stimulation of the lower leg muscles might offer a better tolerated and more physiological alternative to IPCs. In this feasibility trial the investigators will randomly allocate 40 patients to receive either the Geko device (n=20) or IPCs (n=20) as principal means of mechanical VTE prophylaxis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05208216
Study type Interventional
Source Manchester University NHS Foundation Trust
Contact Jonathan Bannard-Smith, MB ChB
Phone 01612761234
Email j.bannardsmith@mft.nhs.uk
Status Recruiting
Phase N/A
Start date November 1, 2022
Completion date May 1, 2024
View Details
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