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PEEP and Spontaneous Breathing During ARDS

Effects of Positive End-expiratory Pressure With and Without Inspiratory Synchronization During Moderate to Severe ARDS

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04241874
Acronym
EARDS
Enrollment
16
Registered
2020-01-27
Start date
2021-05-01
Completion date
2022-06-15
Last updated
2022-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome

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.

Interventions

OTHERMechanical Ventilation

Respiratory support through mechanical ventilator

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
Inspiratory effort45 minutesThe negative deflection in esophageal pressure during inspiration

Secondary

MeasureTime frameDescription
Respiratory mechanics45 minutesRespiratory mechanics assessed by end-inspiratory occlusion
Lung mechanics45 minutesRespiratory mechanics assessed by esophageal pressure monitoring during an end-inspiratory occlusion
Work of breathing45 minutesEsopghageal pressure pressure-time product per minute
Respiratory rate45 minutesRespiratory rate per minute
Regional Tidal volume distribution45 minutesDistribution of tidal volume in the different lung zones, assessed by electrical impedance tomography
Oxygenation45 minutesRatio of PaO2 to FiO2
Pendelluft45 minutesOccurrence of intra-tidal shift of gas within different lung regions at beginning of inspiration
Carbon dioxide45 minutesBlood carbon dioxide, as assessed by arterial blood gas analysis
Tidal volume45 minutesAverage Tidal volume received by the patient
Dynamic transpulmonary driving pressure45 minutesThe average positive swing in transpulmonary driving pressure during tidal breathing
Alveolar recruitment45 minutesChange in end-expiratory lung impedance, assessed by electrical impedance tomography

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026