EARDS: PEEP and Spontaneous Breathing During ARDS

Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Recruiting
CT.gov ID
NCT04241874
Collaborator
(none)
16
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15
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Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Mechanical Ventilation
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
16 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Positive End-expiratory Pressure With and Without Inspiratory Synchronization During Moderate to Severe ARDS
Actual Study Start Date :
May 1, 2021
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Low PEEP and full inspiratory synchronization

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

Other: Mechanical Ventilation
Respiratory support through mechanical ventilator

Experimental: High PEEP and full inspiratory synchronization

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

Other: Mechanical Ventilation
Respiratory support through mechanical ventilator

Experimental: Low PEEP and inspiratory desynchronization

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

Other: Mechanical Ventilation
Respiratory support through mechanical ventilator

Experimental: High PEEP and inspiratory desynchronization

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

Other: Mechanical Ventilation
Respiratory support through mechanical ventilator

Outcome Measures

Primary Outcome Measures

  1. Inspiratory effort [45 minutes]

    The negative deflection in esophageal pressure during inspiration

Secondary Outcome Measures

  1. Oxygenation [45 minutes]

    Ratio of PaO2 to FiO2

  2. Respiratory mechanics [45 minutes]

    Respiratory mechanics assessed by end-inspiratory occlusion

  3. Lung mechanics [45 minutes]

    Respiratory mechanics assessed by esophageal pressure monitoring during an end-inspiratory occlusion

  4. Work of breathing [45 minutes]

    Esopghageal pressure pressure-time product per minute

  5. Respiratory rate [45 minutes]

    Respiratory rate per minute

  6. Regional Tidal volume distribution [45 minutes]

    Distribution of tidal volume in the different lung zones, assessed by electrical impedance tomography

  7. Alveolar recruitment [45 minutes]

    Change in end-expiratory lung impedance, assessed by electrical impedance tomography

  8. Pendelluft [45 minutes]

    Occurrence of intra-tidal shift of gas within different lung regions at beginning of inspiration

  9. Carbon dioxide [45 minutes]

    Blood carbon dioxide, as assessed by arterial blood gas analysis

  10. Tidal volume [45 minutes]

    Average Tidal volume received by the patient

  11. Dynamic transpulmonary driving pressure [45 minutes]

    The average positive swing in transpulmonary driving pressure during tidal breathing

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondazione Policlinico Universitaro A. Gemelli IRCCS Rome Italy

Sponsors and Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Investigators

  • Principal Investigator: Giuseppe Bello, MD, Fondazione Policlinico A. Gemelli IRCCS
  • Study Director: Massimo Antonelli, MD, Fondazione Policlinico A. Gemelli IRCCS

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
ClinicalTrials.gov Identifier:
NCT04241874
Other Study ID Numbers:
  • EARDS
First Posted:
Jan 27, 2020
Last Update Posted:
Mar 25, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 25, 2022