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Effectiveness Study of Electrical Stimulation in Prevention of Decubitus.

Effectiveness Study of Electrical Stimulation in Prevention of Decubitus.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29627
Enrollment
50
Registered
2010-03-23
Start date
2011-05-01
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 electrical stimulation. For each patients it will be randomised which foot receives electrical stimulation for one hour per day.
2. Pulse width 200 milliseconds
3. Output current 6 mA.

Sponsors

Medisch Spectrum Twente Enschede
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Expected stay on the Intensive Care for at least 48 hours; 2. Braden score < 20.

Exclusion criteria

Exclusion criteria: 1. Decubitus ulcer grade 1 – 4 on the heel; 2. Ulcer at the lower leg; 3. Amputation of one or both legs; 4. Difference of more than 25% between both legs in the Ankle Brachial Index; 5. Systolic blood pressure at the foot > 250mmHg; 6. Inability to wear the sock; 7. Dark skin; 8. 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
Incidence of decubitus ulcers of the heel.

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)