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Feasibility of a neuromuscular electrostimulation device for mechanical thromboprophylaxis in ICU patients

Phase 3
Recruiting
Conditions
I74.3
Embolism and thrombosis of arteries of lower extremities
Registration Number
DRKS00015841
Lead Sponsor
Medizinische Universität Wien
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

age = 18 years, Caprini Score = 5 indicating the highest risk of VTE and therefore combined VTE prophylaxis (Enoxaparin 1x40mg + mechanical device)

Exclusion Criteria

patient`s refusal of participation, neuromuscular disorder of the lower limbs, formally prohibition of muscle movement in the lower limb (e.g. after certain surgical procedures), implanted electronic devices (e.g. pacemaker), recently diagnosed or suspected thromboembolic event (especially DVT), local open wound or cancerous lesion, pregnancy, epilepsy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
feasibility, Duration of use of the mechanical device per day
Secondary Outcome Measures
NameTimeMethod
patient compliance, patient comfort, satisfaction of the health care team concerning handling, incidence of procedural problems, costs, incidence of thromboembolic events
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