search
Back to results

PEEP and Spontaneous Breathing During ARDS (EARDS)

Primary Purpose

Acute Respiratory Distress Syndrome

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Mechanical Ventilation
Sponsored by
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Distress Syndrome

Eligibility Criteria

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

Inclusion Criteria:

  • (a) ARDS according to the Berlin definition (ratio of arterial partial pressure of oxygen to fraction of inspired oxygen (PaO2/FiO2) ≤ 300 mmHg);
  • (b) assisted ventilation, as prescribed by the attending physician
  • (c) intense inspiratory effort, defined as a negative deflection in the airway pressure equal or greater than 13 cmH2O in the first breath recorded during an end-expiratory occlusion

Exclusion Criteria:

Pregnancy, clinically documented barotrauma, contraindication to electrical impedance tomography (EIT) use (e.g., presence of pacemaker or automatic implantable cardioverter defibrillator), impossibility to place the EIT belt in the right position (e.g., presence of surgical wounds dressing), and any contraindication to the insertion of a nasogastric tube (eg, recent upper-gastrointestinal surgery, esophageal varices), chest tubes with active air leaks, fever.

Sites / Locations

  • Fondazione Policlinico Universitaro A. Gemelli IRCCS

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Low PEEP and full inspiratory synchronization

High PEEP and full inspiratory synchronization

Low PEEP and inspiratory desynchronization

High PEEP and inspiratory desynchronization

Arm Description

PEEP = 5 cmH2O + clinically selected pressure support (PSVclin)

PEEP = 15 cmH2O + clinically selected pressure support (PSVclin)

PEEP = 5 cmH2O + bilevel positive airway pressure (Respiratory rate 15 breaths/minute, inspiratory time=1 sec, Inspiratory pressure=PSVclin+PEEP, PS=0 cmH2O)

PEEP = 15 cmH2O + bilevel positive airway pressure (Respiratory rate 15 breaths/minute, inspiratory time=1 sec, Inspiratory pressure=PSVclin+PEEP, PS=0 cmH2O)

Outcomes

Primary Outcome Measures

Inspiratory effort
The negative deflection in esophageal pressure during inspiration

Secondary Outcome Measures

Oxygenation
Ratio of PaO2 to FiO2
Respiratory mechanics
Respiratory mechanics assessed by end-inspiratory occlusion
Lung mechanics
Respiratory mechanics assessed by esophageal pressure monitoring during an end-inspiratory occlusion
Work of breathing
Esopghageal pressure pressure-time product per minute
Respiratory rate
Respiratory rate per minute
Regional Tidal volume distribution
Distribution of tidal volume in the different lung zones, assessed by electrical impedance tomography
Alveolar recruitment
Change in end-expiratory lung impedance, assessed by electrical impedance tomography
Pendelluft
Occurrence of intra-tidal shift of gas within different lung regions at beginning of inspiration
Carbon dioxide
Blood carbon dioxide, as assessed by arterial blood gas analysis
Tidal volume
Average Tidal volume received by the patient
Dynamic transpulmonary driving pressure
The average positive swing in transpulmonary driving pressure during tidal breathing

Full Information

First Posted
January 22, 2020
Last Updated
September 4, 2022
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
search

1. Study Identification

Unique Protocol Identification Number
NCT04241874
Brief Title
PEEP and Spontaneous Breathing During ARDS
Acronym
EARDS
Official Title
Effects of Positive End-expiratory Pressure With and Without Inspiratory Synchronization During Moderate to Severe ARDS
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2021 (Actual)
Primary Completion Date
June 15, 2022 (Actual)
Study Completion Date
June 15, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

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
Prospective, physiological study to systematically assess the effects of high positive end-expiratory pressure (PEEP) with and without inspiratory synchronization in patients with moderate to severe acute respiratory distress syndrome (ARDS) exhibiting intense inspiratory effort while on assisted ventilation.
Detailed Description
This prospective, physiological, randomized, cross-over study will be conducted in the 20-bed general ICU of the Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy. Patients with ARDS will be screened for eligibility. ARDS will be defined according to the Berlin Definition. Intubated patients fulfilling ARDS criteria, undergoing assisted ventilation as per clinical decision and exhibiting intense inspiratory effort (occlusion pressure equal or greater than 13 cmH2O) will be enrolled. Patients will be placed in a 30°-45° head up position during all study phases. According to our institution protocol, pressure support setting will be selected by the attending physician to target a predefined tidal volume range of 6-8 mL/kg of predicted body weight (PBW) (female PBW [kg] = 45.5 + 0.91 [cm of height - 152.4]; male PBW [kg] = 50 + 0.91 [cm of height - 152.4]).The lowest pressure support level allowed will be 7 cmH2O, even if Vt <8 ml/Kg PBW is not achieved. In each patient, four different ventilator settings will be applied in a random order. Each step will last 45 minutes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Low PEEP and full inspiratory synchronization
Arm Type
Experimental
Arm Description
PEEP = 5 cmH2O + clinically selected pressure support (PSVclin)
Arm Title
High PEEP and full inspiratory synchronization
Arm Type
Experimental
Arm Description
PEEP = 15 cmH2O + clinically selected pressure support (PSVclin)
Arm Title
Low PEEP and inspiratory desynchronization
Arm Type
Experimental
Arm Description
PEEP = 5 cmH2O + bilevel positive airway pressure (Respiratory rate 15 breaths/minute, inspiratory time=1 sec, Inspiratory pressure=PSVclin+PEEP, PS=0 cmH2O)
Arm Title
High PEEP and inspiratory desynchronization
Arm Type
Experimental
Arm Description
PEEP = 15 cmH2O + bilevel positive airway pressure (Respiratory rate 15 breaths/minute, inspiratory time=1 sec, Inspiratory pressure=PSVclin+PEEP, PS=0 cmH2O)
Intervention Type
Other
Intervention Name(s)
Mechanical Ventilation
Intervention Description
Respiratory support through mechanical ventilator
Primary Outcome Measure Information:
Title
Inspiratory effort
Description
The negative deflection in esophageal pressure during inspiration
Time Frame
45 minutes
Secondary Outcome Measure Information:
Title
Oxygenation
Description
Ratio of PaO2 to FiO2
Time Frame
45 minutes
Title
Respiratory mechanics
Description
Respiratory mechanics assessed by end-inspiratory occlusion
Time Frame
45 minutes
Title
Lung mechanics
Description
Respiratory mechanics assessed by esophageal pressure monitoring during an end-inspiratory occlusion
Time Frame
45 minutes
Title
Work of breathing
Description
Esopghageal pressure pressure-time product per minute
Time Frame
45 minutes
Title
Respiratory rate
Description
Respiratory rate per minute
Time Frame
45 minutes
Title
Regional Tidal volume distribution
Description
Distribution of tidal volume in the different lung zones, assessed by electrical impedance tomography
Time Frame
45 minutes
Title
Alveolar recruitment
Description
Change in end-expiratory lung impedance, assessed by electrical impedance tomography
Time Frame
45 minutes
Title
Pendelluft
Description
Occurrence of intra-tidal shift of gas within different lung regions at beginning of inspiration
Time Frame
45 minutes
Title
Carbon dioxide
Description
Blood carbon dioxide, as assessed by arterial blood gas analysis
Time Frame
45 minutes
Title
Tidal volume
Description
Average Tidal volume received by the patient
Time Frame
45 minutes
Title
Dynamic transpulmonary driving pressure
Description
The average positive swing in transpulmonary driving pressure during tidal breathing
Time Frame
45 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (a) ARDS according to the Berlin definition (ratio of arterial partial pressure of oxygen to fraction of inspired oxygen (PaO2/FiO2) ≤ 300 mmHg); (b) assisted ventilation, as prescribed by the attending physician (c) intense inspiratory effort, defined as a negative deflection in the airway pressure equal or greater than 13 cmH2O in the first breath recorded during an end-expiratory occlusion Exclusion Criteria: Pregnancy, clinically documented barotrauma, contraindication to electrical impedance tomography (EIT) use (e.g., presence of pacemaker or automatic implantable cardioverter defibrillator), impossibility to place the EIT belt in the right position (e.g., presence of surgical wounds dressing), and any contraindication to the insertion of a nasogastric tube (eg, recent upper-gastrointestinal surgery, esophageal varices), chest tubes with active air leaks, fever.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giuseppe Bello, MD
Organizational Affiliation
Fondazione Policlinico A. Gemelli IRCCS
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Massimo Antonelli, MD
Organizational Affiliation
Fondazione Policlinico A. Gemelli IRCCS
Official's Role
Study Director
Facility Information:
Facility Name
Fondazione Policlinico Universitaro A. Gemelli IRCCS
City
Rome
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Individual patient data will be made available upon a reasonable request

Learn more about this trial

PEEP and Spontaneous Breathing During ARDS

We'll reach out to this number within 24 hrs