Clinical Trials Directory

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UnknownNCT02706587

Neuromuscular Electrical Stimulation for Intensive Care Unit-acquired Weakness Assessment

Neuromuscular Electrical Stimulation for Intensive Care Unit-acquired Weakness

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
102 (estimated)
Sponsor
Institut Mutualiste Montsouris · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether early neuromuscular electrical stimulation is effective in the prevention of neuromuscular weakness in critical ill patients.

Detailed description

Randomized, controlled study of early electrical neurostimulation (vs sham) in critically ill patients.

Conditions

Interventions

TypeNameDescription
DEVICENeuromuscular electrical stimulationNEMS is delivered bilaterally to the quadriceps femoris muscle using a portable battery-powered stimulator (Rehab 400, Cefar Compex, France). The electrodes are placed on the motor points of vastus medialis and vastus lateralis muscles. Electrical stimuli of 45Hz (pulse width: 380 µseconds; 6 seconds on with 1.5 second rise time; and 0.75 seconds fall time.; 5 seconds off). The current is adjusted to ensure maximum tolerable muscle contraction The protocol is applied twice daily for 25 minutes, five days a week.
DEVICESham controlNo electrostimulation

Timeline

Start date
2016-03-01
Primary completion
2018-04-01
Completion
2018-06-01
First posted
2016-03-11
Last updated
2016-09-13

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02706587. Inclusion in this directory is not an endorsement.