Lung MORphological Modifications Evaluated by Electrical Impedance Tomography During Preoxygenation for the Intubation of Hypoxemic Patients: Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation (MORPHEIT Study, an Ancillary Study of PREONIV Trial)

Sponsor
University Hospital, Clermont-Ferrand (Other)
Overall Status
Unknown status
CT.gov ID
NCT03282331
Collaborator
(none)
30
1
3
16
1.9

Study Details

Study Description

Brief Summary

Prospective, randomized clinical multicentric study, in ICU, during preoxygenation for the intubation of hypoxemic patients.

Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Condition or Disease Intervention/Treatment Phase
  • Procedure: Standard oxygenation
  • Procedure: High flow nasal oxygenation
  • Procedure: noninvasive ventilation
N/A

Detailed Description

Preoxygenation before endotracheal intubation in the ICU is a prerequisite to limit complications, ranging from desaturation, severe hypoxemia and bradycardia with potential cardiac arrest and death. International recommendations suggest the use of non-invasive ventilation (NIV) technique whenever possible. High flow nasal cannula (HFNC) has recently gained growing interest in the ICU as a treatment of acute respiratory failure, to improve extubation success and as a preoxygenation device before endotracheal intubation. Conflicting results have been published.

The PREONIV study was designed to compare NIV, HFNC and conventional preoxygenation with valve bag mask for the preoxygenation before endotracheal intubation.

Investigator propose to add a lung morphology analysis during preoxygenation. Electrical impedance tomography (EIT) is a non invasive tool which analyse lung aeration variations via the evolution of local thoracic impedances with electrical loop circulating around a thoracic belt with electrodes.

The hypothesis is that the technique of preoxygenation might correlate with oxygen desaturation and potential intubation related complications (PREONIV study). Moreover lung morphology modifications evaluated by EIT might be associated with the preoxygenation technique (MORPHEIT study).

Investigator wish to asses lung morphological modifications evaluated by EIT during preoxygenation in a prospective non blinded randomized fashion.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking Description:
open
Primary Purpose:
Treatment
Official Title:
Lung MORphological Modifications Evaluated by Electrical Impedance Tomography During Preoxygenation for the Intubation of Hypoxemic Patients: Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation (MORPHEIT Study, an Ancillary Study of PREONIV Trial)
Actual Study Start Date :
Jun 2, 2016
Actual Primary Completion Date :
Sep 1, 2017
Anticipated Study Completion Date :
Oct 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: standard oxygenation

Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Procedure: Standard oxygenation
Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Other: High flow nasal oxygen therapy

Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Procedure: High flow nasal oxygenation
Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Other: NonInvasive Ventilation

Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Procedure: noninvasive ventilation
Electrical impedance tomographic evaluation of lung morphology variations according to the preoxygenation technique : Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

Outcome Measures

Primary Outcome Measures

  1. evolution of lung aeration evaluated by electrical impedance tomography during the preoxygenation for intubation of hypoxemic patients and the arterial blood oxygenation [at day 1]

Secondary Outcome Measures

  1. electrical impedance tomography related indexes [at day 1 (before, during and after preoxygenation and at 5 minutes and at 30 minutes after intubation)]

  2. Lung inhomogeneity index [at day 1 (during and after preoxygenation and at 5 minutes and at 30 minutes after intubation)]

  3. End expiratory lung impedance [at day 1 (during and after preoxygenation and at 5 minutes and at 30 minutes after intubation)]

  4. Center of Ventilation [at day 1 (during and after preoxygenation and at 5 minutes and at 30 minutes after intubation)]

  5. Tidal Volume [at day 1 (during and after preoxygenation and at 5 minutes and at 30 minutes after intubation)]

  6. pulse oxymetry value [at day 1 (at 5 minutes and at 30 minutes after intubation)]

  7. Partial pressure of arterial oxygen (PaO2) [at day 1]

  8. Regurgitation rate [at day 1]

  9. oxyhemoglobin desaturation below 80 % [at day 1]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • • adults patients

  • requiring intubation and hypoxemia (defined by PaO2/FiO2 below 200)

  • patient covered by french health care system

  • patient included in Hopital Estaing, Clermont-Ferrand

Exclusion Criteria:
  • • patient refusal

  • intubation for other causes (excluding hypoxemia)

  • impossibility to measure pulse oxymetry value

  • contraindication for NIV : vomiting

  • NIV intolerance

  • cardiac arrest during intubation

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Clermont-Ferrand Clermont-Ferrand France 63003

Sponsors and Collaborators

  • University Hospital, Clermont-Ferrand

Investigators

  • Principal Investigator: Thomas GODET, University Hospital, Clermont-Ferrand

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Clermont-Ferrand
ClinicalTrials.gov Identifier:
NCT03282331
Other Study ID Numbers:
  • CHU-345
  • 2012-A00778-35
First Posted:
Sep 13, 2017
Last Update Posted:
Sep 14, 2017
Last Verified:
Sep 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Clermont-Ferrand
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 14, 2017