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Clinical Trials/NCT05035290
NCT05035290
Recruiting
Not Applicable

Negative Pressure Ventilation in Critically Ill Paediatric Patients During Weaning: Prospective Randomized Interventional Trial

Brno University Hospital1 site in 1 country200 target enrollmentFebruary 1, 2022
ConditionsWeaning Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Weaning Failure
Sponsor
Brno University Hospital
Enrollment
200
Locations
1
Primary Endpoint
Early weaning failure
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Negative pressure ventilation (NPV) represent a unique form of noninvasive ventilation using negative pressure by specialized cuirass, that evolve negative pressure on the front size of chest and partially abdomen and facilitate the spontaneous breathing. The benefit of NPV beside noninvasive application, is the supreme tolerance of the patient (compared to other forms of noninvasive ventilation - mask, helmet), without the negative impact on enteral feeding tolerance and with the possibility of active physiotherapy. NPV could be even combined with oxygentherapy or noninvasive positive pressure ventilation. NPV in paediatric patients after extubation could be associated with reduced incidence of weaning failure.

Detailed Description

After ethics committee approval and informed consent from legal guardians and fulfilling inclusion criteria, critically ill paediatric patients scheduled for weaning will be randomized (in 1:1 allocation) to NPV (interventional group) or standard approach (without NPV) after extubation. NPV in paediatric patients after extubation could be associated with reduced incidence of weaning failure. The initial setting on NPV will be: negative pressure set to -10cmH2O and will proceed for minimal time of 60 minutes after extubation (will proceed longer in case of good tolerance). In case of hypoxaemia, additional oxygentherapy will be administered according to the patients condition Primary outcome will be defined as postextubation failure incidence at 60 minutes after extubation (defined as need of noninvasive positive pressure ventilation, intubation, or high-flow oxygen therapy) and the overall incidence of weaning failure during initial 24 hour after extubation. The secondary outcome will be the dynamics of blood gases (arterial or capillary blood sample) during initial 60 minutes after extubation (1. extubation, 2. 60 minutes after extubation) and the need of and amount of artificial oxygentherapy (litres of oxygen per minute, pulse oximetry). Another outcome will be the overall cuirass tolerance after 60 minutes and after 24 hours defined by incidence of skin lesions.

Registry
clinicaltrials.gov
Start Date
February 1, 2022
End Date
December 31, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Brno University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Petr Štourač, MD

Clinical Professor

Brno University Hospital

Eligibility Criteria

Inclusion Criteria

  • invasive mechanical ventilation
  • informed consent
  • scheduled for weaning

Exclusion Criteria

  • neuromuscular disorder
  • mechanical ventilation at home (chronic use)
  • less than 24 hours after abdominal or thoracic surgery
  • technical problems with the cuirass - chest drain

Outcomes

Primary Outcomes

Early weaning failure

Time Frame: in 60 minutes after extubation

Incidence of early weaning failure - intubation, noninvasive positive pressure ventilation, high flow oxygen therapy

Overall weaning failure

Time Frame: during 24 hours after extubation

Incidence of weaning failure - intubation, noninvasive positive pressure ventilation, high flow oxygen therapy

Secondary Outcomes

  • Overall cuirass tolerance(during 24 hours after extubation)
  • Blood gases trends(during initial 60 minutes after extubation)
  • Early cuirass tolerance(during initial 60 minutes after extubation)
  • Pulse oximetry trend(during initial 60 minutes after extubation)

Study Sites (1)

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