Post-Extubation Assessment of Clinical Stability in ELBW Infants

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 28
SponsorMcGill University Health Centre/Research Institute of the McGill University Health Centre

About this trial

This is an observational, proof-of-concept, feasibility study that aims to evaluate the feasibility of a monitoring system that integrates clinical data, high-resolution waveforms from the bedside monitor, regional oxygenation (via cerebral and splanchnic near-infrared spectroscopy), and regional ventilation (via electrical impedance tomography) from 20 extremely low birth weight infants at high-risk of reintubation.

Eligibility criteria

Qualifiers

Birth weight < 1000g and gestational age < 28+0 weeks,

Received mechanical ventilation within the first 72h of life,

Undergoing their first planned extubation within the first 6 weeks of life.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Oxygen saturation probe
  • Near infrared spectroscopy sensors
  • Electrical impedance tomography

Treatment groups

20 Participants
are divided into 1 treatment group