RecruitingNANCT04068012

A Computerized Decision Support Tool for Ventilator Management in Pediatric Acute Respiratory Distress Syndrome Pilot Study

Sponsor: Children's Hospital Los Angeles

Trial Details

ConditionVentilation Therapy; Complications, Ventilator-Induced Lung Injury, Ards
InterventionVentilator protocol
PhaseNA
StatusRecruiting
Participants180
Est. Completion1 July 2027
Last Updated14 Apr 2026

Primary Outcome

Aim 1: Implementation Feasibility; Aim 2: Protocol Adherence

Eligibility Criteria

Inclusion Criteria

Inclusion Criteria: * Children \> 1 month of age and \>44 weeks gestation and ≤ 18 years of age AND * Supported on mechanical ventilation with pulmonary parenchymal disease (i.e. Pediatric Acute Respiratory Distress Syndrome (PARDS)) with Oxygen Saturation Index (OSI) ≥ 5) or Oxygenation Index (OI) ≥ 4 AND * Who are within 72 hours of initiation of invasive mechanical ventilation AND * Who are anticipated to require \>72 hours mechanical ventilation. Exclusion Criteria: * Conditions on enrollment that preclude conventional methods of weaning (i.e., status asthmaticus, severe lower airway obstruction, bronchiolitis, critical airway, Extra Corporeal Life Support (ECLS), intubation for Upper Airway Obstruction, Do Not Resuscitate orders, severe chronic respiratory failure, spinal cord injury above lumbar region, cyanotic heart disease (unrepaired or palliated)) OR * Conditions precluding the use of permissive hypercapnia or hypoxemia (i.e. intracranial hypertension, severe pulmonary hypertension) * Primary Attending physician refuses to enroll the patient

Trial Sites

Countries

United StatesCanadaItaly
View Registry Entry

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