MedPath

Comfort and Safety Study of Electrical Stimulation in Prevention of Decubitus.

Completed
Conditions
Decubitus
Registration Number
NL-OMON24045
Lead Sponsor
Medisch Spectrum Twente
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
25
Inclusion Criteria

1. Patients who are admitted to the vascular surgery ward (C3) of Medisch Spectrum Twente;

2. Expected stay on the vascular surgery ward for at least 3 days, excluding weekend days.

Exclusion Criteria

1. Decubitus ulcer grade 1 – 4 on the heel;

2. Ulcer or surgical wound at the lower leg;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary objectives of this study are:<br /><br>1. Will there be any adverse events, due to the electrical stimulation?<br /><br>2. Are the sock and the electrical stimulation comfortable for the patient?
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath