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N/A Completed N=150 Randomized Double-blind Prevention

Preoxygenation With Positive Inspiratory Pressure During Induction of Anesthesia

Anesthesia
Source: ClinicalTrials.gov NCT02313766 ↗
Enrolled (actual)
150
Serious AEs
0.0%
Results posted
Jan 2015
Primary outcomePrimary: Time for Preoxygenationfrom Face Mask Positioning to FEO2=90% — 190; 153; 140 seconds

Summary

Adults patients scheduled for elective surgery were randomly allocated to receive preoxygenation with spontaneous breathing, positive pressure ventilation (positive inspiratory pressure: 12 cmH2O) without PEEP, and with PEEP (positive inspiratory pressure: 12 cmH2O, PEEP: 6 cmH2O). Preoxygenation time was measured from face mask positioning to FEO2=90% (FEO2 : expired fraction of O2). After endotracheal tube placement the time until SpO2=93% (SpO2 : peripheral oxygen saturation) was measured during monitored apnoea. Patient's discomfort was recorded (visual analogue scale).

Outcome Measures

OutcomeResultp-value
PRIMARY
Time for Preoxygenationfrom Face Mask Positioning to FEO2=90%
190; 153; 140
SECONDARY
Time Until SpO2=93%
305; 370; 345
SECONDARY
Discomfort of the Preoxygenation Phase Self Reported by the Patient
0; 8; 0

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) physical status I and II
  • Scheduled surgery with general anaesthesia and oro-tracheal intubation

Exclusion Criteria

  • rapid sequence induction
  • anticipated difficult mask ventilation
  • anticipated difficult intubation
  • refusal to participate to the study and to sign informed consent
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02313766). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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