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Prone Position in Patients on High-flow Nasal Oxygen Therapy for COVID-19 (HIGH-PRONE-COVID-19)

Primary Purpose

Acute Respiratory Distress Syndrome, COVID-19

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Prone decubitus
Sponsored by
University Hospital, Tours
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Distress Syndrome focused on measuring Acute Respiratory Distress Syndrome, COVID-19, SARS-CoV-2, Nasal High-Flow, Prone position

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patient
  • with COVID-19 pneumonia according to the diagnostic criteria in effect at the time of inclusion or very highly suspected.
  • Patient treated with nasal high-flow
  • Mild, moderate or severe ARDS: bilateral radiological opacities not fully explained by effusions, atelectasis or nodules; acute hypoxemia with worsening within the previous 7 days, not fully explained by left ventricular failure; PaO2/FiO2 ratio < 300 mmHg (or equivalent SpO2/FiO2).
  • Covered by or having the rights to French social security
  • Informed Consent

Exclusion Criteria:

Pregnant or breastfeeding woman

  • Indication for immediate tracheal intubation
  • Progressive significant acute circulatory insufficiency
  • Impaired alertness, confusion, restlessness
  • Body mass index > 40 kg/m2
  • Thoracic trauma or other contraindication to prone position
  • Pneumothorax with single anterior thoracic drain and persistent bubbling
  • Vulnerable person: safeguard of justice, guardianship or authorship known at inclusion

Sites / Locations

  • Intensive Care Unit, University Hospital, Aix
  • Medical Intensive Care Unit, University Hospital, Amiens
  • Intensive Care Unit, Hospital, Argenteuil
  • Intensive Care Unit, Hospital,
  • Medical Intensive Care Unit, University Hospital, Brest
  • Medical Intensive Care Unit, Hospital, Béthune
  • Medical Intensive Care Unit, University Hospital, Caen
  • Intensive Care Unit, Louis Mourier-APHP
  • Intensive Care Unit, Hospital, Dax
  • Medical Intensive Care Unit, University Hospital, Dijon
  • Medical Intensive Care Unit, University Hospital, Grenoble
  • Intensive Care Unit, Hospital, La Roche-sur-Yon
  • Intensive Care Unit, Hospital, Le Mans
  • Intensive Care Unit, University Hospital, Lille
  • Medical Intensive Care Unit, University Hospital, Nantes
  • Medical Intensive Care Unit, University Hospital, Nice
  • Medical Intensive Care Unit, Hospital, Orléans
  • Medical Intensive Care Unit, Tenon-APHP
  • Medical Intensive Care Unit, University Hospital, Poitiers
  • Medical Intensive Care Unit, University Hospital, Tours
  • Surgical Intensive Care Unit, University Hospital, Tours
  • Intensive Care Unit, Hospital, Valence
  • Medical Intensive Care Unit, University Hospital, Nancy
  • Intensive Care Unit, Hospital, Vannes

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Prone decubitus group

Control group

Arm Description

Prone positioning of patients on nasal high-flow oxygen therapy with usual care

Patients on nasal high-flow oxygen therapy with usual care and positioned in supine

Outcomes

Primary Outcome Measures

Therapeutic failure within 14 days of randomization
Therapeutic failure is defined by death or intubation or use of non-invasive ventilation at two pressure levels.

Secondary Outcome Measures

Therapeutic failure within 28 days of randomization
Therapeutic failure is defined by death or intubation or use of non-invasive ventilation at two pressure levels.
Timeframe of intubation or death
Timeframe of therapeutic escalation (in case of non-invasive ventilation at two pressure levels)
Evolution of oxygenation (PaO2/FiO2 ratio or SpO2/FiO2 surrogate) over the 14 days following randomization
Evolution of the SpO2/FiO2 ratio during the first prone session
Evolution of the ROX index during the first prone session
ROX index is the ratio of pulse oximetry (SpO2)/fraction of inspired oxygen (FiO2) to respiratory rate.
Evolution of the World Health Organization disease severity score of COVID
Score reaches from 1 to 7, 7 indicates worse outcome
Patient comfort before, during and after the first prone position session
Comfort evaluted by the patient through a visual analogical scale
Occurrence of skin lesions on the anterior surface of the body
Displacement of invasive devices during reversals
Invasive devices include : central and peripheric vascular catheters, tracheal tube, urinary catheter, chest tubes.
Days of nasal High-Flow therapy use in the general population, in non-intubated patients and in intubated patients
Days spent in the intensive care unit and in the hospital
Mortality in the intensive care unit and in the hospital
Ventilator-free-days within 28 days of randomization

Full Information

First Posted
April 16, 2020
Last Updated
April 15, 2021
Sponsor
University Hospital, Tours
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1. Study Identification

Unique Protocol Identification Number
NCT04358939
Brief Title
Prone Position in Patients on High-flow Nasal Oxygen Therapy for COVID-19 (HIGH-PRONE-COVID-19)
Official Title
Evaluation of Prone Position in Conscious Patients on Nasal High-flow Oxygen Therapy for COVID-19 Disease Induced Acute Respiratory Distress Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
April 27, 2020 (Actual)
Primary Completion Date
February 21, 2021 (Actual)
Study Completion Date
February 21, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Tours

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Acute Respiratory Distress Syndrome (ARDS) induces high mortality, particularly in the context of COVID-19 disease. Preliminary data from patients with ARDS related to COVID-19 disease appear to show significant effectiveness of prone positioning in intubated patients in terms of oxygenation as well as nasal high flow therapy before intubation. It should be noted that in Jiangsu province, secondarily affected, nasal high flow combined with the prone position was successfully integrated into care protocols. The investigators hypothesize that the combined application of nasal high flow and prone positioning can significantly improve the outcome of patients suffering from COVID-19 pneumonia by reducing the need for tracheal intubation and associated therapeutics such as sedation and paralysis, resulting in both individual and collective benefits in terms of use of scarce critical care resources. Investigators hypothesize that the combined application of nasal high-flow and prone positioning can significantly improve the outcome of patients suffering from COVID-19 pneumonia by reducing the need for intubation and associated therapeutics such as sedation and paralysis, resulting in both individual and collective benefits in terms of use of scarce critical care resources.
Detailed Description
Acute Respiratory Distress Syndrome (ARDS) induces high mortality, particularly in the context of COVID-19 disease. In patients with ARDS who are mechanically ventilated invasively through a tracheal tube and with a PaO2/FiO2 ratio (arterial oxygen partial pressure to inspired oxygen fraction ratio) of less than 150 mmHg, prone positioning significantly reduced mortality. Furthermore, nasal high flow, a non-invasive respiratory support and oxygenation technique, reduced the need for tracheal intubation and reduced mortality among the most severe patients (PaO2/FiO2 ratio less than 200 mmHg) suffering from acute hypoxemic respiratory failure. Prone positioning of ARDS patients treated with nasal high-flow was evaluated in 20 patients with predominantly viral pneumonia. The prone positioning was found to be feasible and associated with an increased PaO2/FiO2 ratio. Preliminary data from patients with ARDS related to COVID-19 disease appear to show a significant effect of prone positioning in intubated patients in terms of oxygenation improvement as well as nasal high-high flow appears effective in non-intubated patients. For instance, nearly half intensive care unit patients described in the princeps cohort in Wuhan City, Hubei Province, China, had received nasal high-flow. It should be noted that in Jiangsu province, secondarily affected, nasal high-flow combined with prone positioning was successfully integrated into care protocols. Investigators hypothesize that the combined application of nasal high-flow and prone positioning can significantly improve the outcome of patients suffering from COVID-19 pneumonia by reducing the need for intubation and associated therapeutics such as sedation and paralysis, resulting in both individual and collective benefits in terms of use of scarce critical care resources.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome, COVID-19
Keywords
Acute Respiratory Distress Syndrome, COVID-19, SARS-CoV-2, Nasal High-Flow, Prone position

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
405 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prone decubitus group
Arm Type
Experimental
Arm Description
Prone positioning of patients on nasal high-flow oxygen therapy with usual care
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients on nasal high-flow oxygen therapy with usual care and positioned in supine
Intervention Type
Other
Intervention Name(s)
Prone decubitus
Intervention Description
According to the tolerance, the objective is to spend as much time as possible, up to 16 hours and beyond in prone position every 24 hours. At least two sessions of at least 30 minutes each must be performed daily.
Primary Outcome Measure Information:
Title
Therapeutic failure within 14 days of randomization
Description
Therapeutic failure is defined by death or intubation or use of non-invasive ventilation at two pressure levels.
Time Frame
From randomization to day 14
Secondary Outcome Measure Information:
Title
Therapeutic failure within 28 days of randomization
Description
Therapeutic failure is defined by death or intubation or use of non-invasive ventilation at two pressure levels.
Time Frame
From randomization to day 28
Title
Timeframe of intubation or death
Time Frame
From randomization to day 28
Title
Timeframe of therapeutic escalation (in case of non-invasive ventilation at two pressure levels)
Time Frame
From randomization to day 28
Title
Evolution of oxygenation (PaO2/FiO2 ratio or SpO2/FiO2 surrogate) over the 14 days following randomization
Time Frame
From randomization to day 14
Title
Evolution of the SpO2/FiO2 ratio during the first prone session
Time Frame
From randomization to day 1
Title
Evolution of the ROX index during the first prone session
Description
ROX index is the ratio of pulse oximetry (SpO2)/fraction of inspired oxygen (FiO2) to respiratory rate.
Time Frame
From randomization to day 1
Title
Evolution of the World Health Organization disease severity score of COVID
Description
Score reaches from 1 to 7, 7 indicates worse outcome
Time Frame
From randomization to day 28
Title
Patient comfort before, during and after the first prone position session
Description
Comfort evaluted by the patient through a visual analogical scale
Time Frame
From randomization to day 1
Title
Occurrence of skin lesions on the anterior surface of the body
Time Frame
From randomization to day 28
Title
Displacement of invasive devices during reversals
Description
Invasive devices include : central and peripheric vascular catheters, tracheal tube, urinary catheter, chest tubes.
Time Frame
From randomization to day 28
Title
Days of nasal High-Flow therapy use in the general population, in non-intubated patients and in intubated patients
Time Frame
From randomization to day 28
Title
Days spent in the intensive care unit and in the hospital
Time Frame
From randomization to day 28
Title
Mortality in the intensive care unit and in the hospital
Time Frame
From randomization to day 28
Title
Ventilator-free-days within 28 days of randomization
Time Frame
From randomization to day 28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patient with COVID-19 pneumonia according to the diagnostic criteria in effect at the time of inclusion or very highly suspected. Patient treated with nasal high-flow Mild, moderate or severe ARDS: bilateral radiological opacities not fully explained by effusions, atelectasis or nodules; acute hypoxemia with worsening within the previous 7 days, not fully explained by left ventricular failure; PaO2/FiO2 ratio < 300 mmHg (or equivalent SpO2/FiO2). Covered by or having the rights to French social security Informed Consent Exclusion Criteria: Pregnant or breastfeeding woman Indication for immediate tracheal intubation Progressive significant acute circulatory insufficiency Impaired alertness, confusion, restlessness Body mass index > 40 kg/m2 Thoracic trauma or other contraindication to prone position Pneumothorax with single anterior thoracic drain and persistent bubbling Vulnerable person: safeguard of justice, guardianship or authorship known at inclusion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yonatan PEREZ, MD
Organizational Affiliation
No affiliation
Official's Role
Study Director
Facility Information:
Facility Name
Intensive Care Unit, University Hospital, Aix
City
Aix-en-Provence
ZIP/Postal Code
13616
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Amiens
City
Amiens
ZIP/Postal Code
80054
Country
France
Facility Name
Intensive Care Unit, Hospital, Argenteuil
City
Argenteuil
ZIP/Postal Code
95100
Country
France
Facility Name
Intensive Care Unit, Hospital,
City
Blois
ZIP/Postal Code
41016
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Brest
City
Brest
ZIP/Postal Code
29609
Country
France
Facility Name
Medical Intensive Care Unit, Hospital, Béthune
City
Béthune
ZIP/Postal Code
62408
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Caen
City
Caen
ZIP/Postal Code
14033
Country
France
Facility Name
Intensive Care Unit, Louis Mourier-APHP
City
Colombes
ZIP/Postal Code
92700
Country
France
Facility Name
Intensive Care Unit, Hospital, Dax
City
Dax
ZIP/Postal Code
40107
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Dijon
City
Dijon
ZIP/Postal Code
21033
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Grenoble
City
Grenoble
Country
France
Facility Name
Intensive Care Unit, Hospital, La Roche-sur-Yon
City
La Roche-sur-Yon
ZIP/Postal Code
85925
Country
France
Facility Name
Intensive Care Unit, Hospital, Le Mans
City
Le Mans
ZIP/Postal Code
72037
Country
France
Facility Name
Intensive Care Unit, University Hospital, Lille
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Nice
City
NIce
ZIP/Postal Code
06202
Country
France
Facility Name
Medical Intensive Care Unit, Hospital, Orléans
City
Orléans
ZIP/Postal Code
45067
Country
France
Facility Name
Medical Intensive Care Unit, Tenon-APHP
City
Paris
ZIP/Postal Code
75020
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Poitiers
City
Poitiers
ZIP/Postal Code
86021
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Tours
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Name
Surgical Intensive Care Unit, University Hospital, Tours
City
Tours
ZIP/Postal Code
37170
Country
France
Facility Name
Intensive Care Unit, Hospital, Valence
City
Valence
ZIP/Postal Code
26953
Country
France
Facility Name
Medical Intensive Care Unit, University Hospital, Nancy
City
Vandœuvre-lès-Nancy
ZIP/Postal Code
54511
Country
France
Facility Name
Intensive Care Unit, Hospital, Vannes
City
Vannes
ZIP/Postal Code
56017
Country
France

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data after de-identification can be obtained by contacting the corresponding author.
IPD Sharing Time Frame
Data will be available immediately following publication and ending in 5 years.
IPD Sharing Access Criteria
Contact with the corresponding author.
Citations:
PubMed Identifier
34425070
Citation
Ehrmann S, Li J, Ibarra-Estrada M, Perez Y, Pavlov I, McNicholas B, Roca O, Mirza S, Vines D, Garcia-Salcido R, Aguirre-Avalos G, Trump MW, Nay MA, Dellamonica J, Nseir S, Mogri I, Cosgrave D, Jayaraman D, Masclans JR, Laffey JG, Tavernier E; Awake Prone Positioning Meta-Trial Group. Awake prone positioning for COVID-19 acute hypoxaemic respiratory failure: a randomised, controlled, multinational, open-label meta-trial. Lancet Respir Med. 2021 Dec;9(12):1387-1395. doi: 10.1016/S2213-2600(21)00356-8. Epub 2021 Aug 20.
Results Reference
derived
PubMed Identifier
33177145
Citation
Tavernier E, McNicholas B, Pavlov I, Roca O, Perez Y, Laffey J, Mirza S, Cosgrave D, Vines D, Frat JP, Ehrmann S, Li J. Awake prone positioning of hypoxaemic patients with COVID-19: protocol for a randomised controlled open-label superiority meta-trial. BMJ Open. 2020 Nov 11;10(11):e041520. doi: 10.1136/bmjopen-2020-041520.
Results Reference
derived

Learn more about this trial

Prone Position in Patients on High-flow Nasal Oxygen Therapy for COVID-19 (HIGH-PRONE-COVID-19)

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