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Clinical Trials/ACTRN12613001216707
ACTRN12613001216707
Recruiting
未知

A randomised controlled trial studying the effectiveness of mask ventilation with a 2 person method compared to the mask ventilation with a 1 person method in preterm neonates prior to non-emergent endotracheal intubation in reducing mask leak and airway obstruction

Westmead Hospital0 sites60 target enrollmentNovember 5, 2013
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Westmead Hospital
Enrollment
60
Status
Recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 5, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Westmead Hospital

Eligibility Criteria

Inclusion Criteria

  • •1\. Gestation less than 30 weeks
  • •2\. Undergoing non\-emergent endotracheal intubation in the neonatal intensive care unit for any one of the following indications:
  • •a. Recurrent episodes of apnoea
  • •b. Rapidly rising oxygen requirement or oxygen requirement more than 40% on nasal continuous positive airway pressure of 8 cm H2O
  • •c. Respiratory acidosis with pH less than 7\.25 and PaCO2 more than 55 mm Hg
  • •d. Increasing work of breathing such that in the opinion of the treating neonatologist, the neonate in likely to exhaust himself/herself
  • •e. Large airway leak in an already intubated neonate where ongoing ventilation is required. A larger endotracheal tube will be inserted in this situation.

Exclusion Criteria

  • •1\. Neonates with lethal congenital anomalies
  • •2\. Neonates with upper airway anomalies
  • •3\. Intubation required urgently (cardiorespiratory instability)
  • •4\. Unavailability of the research team

Outcomes

Primary Outcomes

Not specified

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