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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 - Comfort and Safety of Electrical Stimulation in Decubitus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34716
Enrollment
25
Registered
2010-05-20
Start date
2010-05-31
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Decubitus

Interventions

The patient will wear both socks 1 hour a day, for 3 days. The right foot will receive the electrical stimulation. The total time of wearing the sock and receiving electrical stimulation will be 3 h

Sponsors

Medisch Spectrum Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Expected stay on the vascular surgery ward for at least 3 days, excluding weekend days

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Main study parameter/endpoint is the number of occurrences of any kind of discomfort or adverse event due to the sock or electrical stimulation.

Secondary

MeasureTime frame
None

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)