Surface electromyography of the diaphragm on the intensive care unit: A pilot study

Surface electromyography of the diaphragm on the intensive care unit: A pilot study - SEDICU

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON40797

Enrollment

120

Registered

2014-08-22

Start date

2014-09-16

Completion date

Unknown

Last updated

2024-06-11

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

Conditions

diaphragm weakness

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Informed consent Age 18 years Expected duration of mechanical ventilation for * 48 hours

Exclusion criteria

Exclusion criteria: (Suspected) neuromuscular disease (other than ICU-AW) or cervical spinal cord injury Known phrenic nerve injury Contraindication for electrode placement (e.g. severe skin infection at electrode site)

Design outcomes

Primary

Measure	Time frame
* Feasibility * Correlation of transcutaneous sEMG of the diaphragm with EAdi signal of NAVA catheter. * Correlation of transcutaneous sEMG of the diaphragm with airway pressure and flow to detect patient * ventilator dyssynchrony * Changes in sEMG signals during increased physical activity * Correlation of sEMG fatigue parameters with clinical parameters of fatigue during weaning from mechanical ventilation	—

Measure

Time frame

* Feasibility * Correlation of transcutaneous sEMG of the diaphragm with EAdi signal of NAVA catheter. * Correlation of transcutaneous sEMG of the diaphragm with airway pressure and flow to detect patient * ventilator dyssynchrony * Changes in sEMG signals during increased physical activity * Correlation of sEMG fatigue parameters with clinical parameters of fatigue during weaning from mechanical ventilation

—

Secondary

Measure	Time frame
* Weaning failure parameters * Patient experience of respiratory fatigue and nurses* estimate of respiratory fatigue of the patient	—

Countries

Netherlands

Outcome results