Skip to content

Transpulmonary Driving Pressure in ARDS COVID19 Patients

Transpulmonary Driving Pressure in ARDS COVID19 Patients / TRANSPULMONARY-COVID19

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04381286
Acronym
TRANSPULMONARY
Enrollment
40
Registered
2020-05-08
Start date
2019-04-01
Completion date
2021-12-31
Last updated
2020-05-12

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

Conditions

COVID-19, Mechanical Ventilation, SARS-CoV-2

Keywords

elastance, Acute respiratory distress syndrome, Esophageal pressure, Pleural pressure

Brief summary

A majority (65-85%) of critically ill patients admitted in intensive care units with a confirmed diagnostic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) developed an acute respiratory distress syndrome (ARDS) according to BERLIN criteria. Gattinoni et al. recently described that the ARDS related to SARS-CoV-2 was not a Typical ARDS. Patients affected by this infection present indeed a major hypoxemia, which was surprisingly associated in early phase with a high compliance of respiratory system, more than 50 ml/cm H2O in most cases. The cornerstone of current treatment in case of ARDS is the use of lung protective ventilation, including limited tidal volumes (VT), low end-inspiratory plateau pressures while maintaining sufficiently-high positive end-expiratory pressures (PEEP). However, high levels of PEEP in patients may have detrimental effects on hemodynamic status and fluid retention, particularly when the respiratory system compliance is normal. High PEEP may also lead to overdistension and an increase of alveolar dead space. The airway pressures commonly monitored does not reliably reflect the impact of pressures on the lung parenchyma. Elastance of chest wall may indeed largely influence values of airways pressions. In contrast, transpulmonary pressure obtained using esophageal pressure (Pes) directly reflect lung overdistension risk and lung properties. In order to better understand this new kind of ARDS characterized by modest recruitable profile and to better personalize mechanical ventilation setting and therapy it is obvious to precise transpulmonary pressure.

Interventions

None listed

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Major patients (18-90 years old) * Hospitalized following SARS-CoV-2 * Mechanical ventilatory support

Exclusion criteria

* Minor patients

Design outcomes

Primary

MeasureTime frameDescription
Duration of mechanical Ventilation1 dayDuration of mechanical Ventilation

Secondary

MeasureTime frameDescription
Number of Participants with during of Acute respiratory distress syndrom (SDRA)1 dayNumber of Participants with during of Acute respiratory distress syndrom (SDRA)
Length of stay in intensive care unit1 dayLength of stay in intensive care unit
Mortality1 dayMortality
number of patients with pulmonary complications1 daynumber of patients with pulmonary complications
Number of Participants with pulmonary stress and strain1 dayNumber of Participants with pulmonary stress and strain

Countries

France

Contacts

Primary ContactRamin Séverin, MD
s-ramin@chu-montpellier.fr46733825

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026