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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24045
Enrollment
25
Registered
2010-03-23
Start date
2010-05-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Decubitus

Interventions

The patients will wear a sock on each foot that contains electrodes for electrostimulation. The right foot will be stimulated three times one hour in three days. The left foot will only wear the sock

Sponsors

Medisch Spectrum Twente
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: 1. Decubitus ulcer grade 1 – 4 on the heel; 2. Ulcer or surgical wound at the lower leg; 3. Amputation of one or both legs; 4. Inability to wear the sock; 5. Dark skin; 6. Other exclusion criteria included any of the following medical conditions for which electrical stimulation is contraindicated { Houghton PE, Campbell KE; 2001}: A. Ventricular arrhythmia; B. Atrial fibrillation; C. Cardiac pacemaker; D. History of deep radiation therapy within the local region; E. Superficial metal ions or metal implants near the area; F. Pregnancy.

Design outcomes

Primary

MeasureTime frame
The primary objectives of this study are: 1. Will there be any adverse events, due to the electrical stimulation? 2. Are the sock and the electrical stimulation comfortable for the patient?

Contacts

Public ContactJ. Palen, van der

Medisch Spectrum Twente, P.O. Box 50000

+31 (0)53 4872023

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)