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The acute metabolic and cardio respiratory effects of neuromuscular electrical stimulation in critically ill, mechanically ventilated patients: a pilot study.

The acute metabolic and cardio respiratory effects of neuromuscular electrical stimulation in critically ill, mechanically ventilated patients: a pilot study. - Neuromuscular electrical stimulation in critically ill patients (NMES-ICU)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON44494
Enrollment
11
Registered
2014-08-06
Start date
2014-11-01
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

ICU acquired weakness critical illness polyneuropathy nerve damage as a result of critical illness

Interventions

NMES twice a day, for 2 days

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - older than 18 years - sedated (all levels of sedation) or not yet responsive (Ramsay 5-6) - Volume supported or pressure supported mechanically ventilated - respiratory and hemodynamically stable - signed formed consent by legal representative

Exclusion criteria

Exclusion criteria: - known systemic neuromuscular disease (eg, Guillain-Barre syndrome) - ability to actively move the legs - life expectancy less than 24 hours determined by the physician - in contact isolation - pacemaker or implanted cardiac defibrillator - pregnancy - body mass index of > 35kg/m2 - condition in the lower extremity preventing treatment (Skin lesions, fractures, amputations, known or suspected malignancy in the legs, myopathy, paresis of the stimulated muscles, epilepsy, allergic reactions to the electrodes, peripheral edemas counteracting NMES, heavy ischaemia of the lower extremities - corticosteroids usage (>7.5mg/day >3 months) - positive end-expiratory pressure (PEEP) > 14 cmH2O, Fraction of inspired oxygen (FiO2) >0.6 and the presence of air leakage (Haugen, Chan, & Li, 2007) (Kho et al., 2012, Gruther et al., 2010). - patients that receive therapeutic hypothermia

Design outcomes

Primary

MeasureTime frame
To evaluate the effects of NMES on energy expenditure

Secondary

MeasureTime frame
To evaluate the effects of NMES on: - Muscle contraction size as indication of muscle fatigue - Hemodynamics: Blood pressure and heart rate measured continuously - Breathing frequency To evaluate the effects of NMES on safety parameters: - Presence or development of metabolic acidosis (pH

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)