Status:

COMPLETED

Comparison of Two FiO2 (1 or 0.5) for Tracheal Extubation in Post-anesthesia Care Unit

Lead Sponsor:

University Hospital, Caen

Conditions:

Anesthesia

Atelectasis

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of the study is to assess the optimal fraction of inspired oxygen (0.5 or 1) for extubation or removal of a supraglottic airway device after general anesthesia.

Detailed Description

During pre-anesthesia visit, eligible patients receive oral and written information of the study and potential risks. In the operating room all patients giving a written informed consent will undergo...

Eligibility Criteria

Inclusion

  • Patients undergoing general anesthesia, with invasive mechanical ventilation including an airway device (supraglottic airway device or tracheal tube) at their arrival in PACU.
  • ASA physical status classification 1, 2, or 3 stabilized.
  • Surgery performed in emergency operating room department including vascular, digestive, urological and minor trauma surgery or surgery performed in head and neck anesthesia pole block including anterior cervical spine, lumbar disc herniation, cranioplasty, nerve stimulator, vertebroplasty, narrow lumbar canal, simple arthrodesis (less than or equal to two stages), otological, ophthalmological and skin surgery.

Exclusion

  • Per-operative hemodynamic instability.
  • Patients with a BMI greater than 35.
  • Patients classified as difficult to intubate and / or ventilate.
  • Heavy surgeries (operating time greater than 4 hours).
  • Patient requiring postoperative non invasive mechanical ventilation
  • Patients with diagnosed COPD
  • SPO2 in room air \< 96% before the intervention.
  • Any patient under guardianship.
  • Pre-operative and / or intra-operative morphine intake.
  • Surgical management of the upper airways (ex : tonsillectomy)
  • Pregnant and lactating women.

Key Trial Info

Start Date :

April 9 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 16 2021

Estimated Enrollment :

119 Patients enrolled

Trial Details

Trial ID

NCT04879290

Start Date

April 9 2021

End Date

August 16 2021

Last Update

November 3 2021

Active Locations (1)

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1

University Hospital, Caen

Caen, France, 14033