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Clinical Trials/NCT04381286
NCT04381286
Unknown
Not Applicable

Transpulmonary Driving Pressure in ARDS COVID19 Patients / TRANSPULMONARY-COVID19

University Hospital, Montpellier1 site in 1 country40 target enrollmentApril 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mechanical Ventilation
Sponsor
University Hospital, Montpellier
Enrollment
40
Locations
1
Primary Endpoint
Duration of mechanical Ventilation
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 1, 2019
End Date
December 31, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Duration of mechanical Ventilation

Time Frame: 1 day

Duration of mechanical Ventilation

Secondary Outcomes

  • Number of Participants with during of Acute respiratory distress syndrom (SDRA)(1 day)
  • Length of stay in intensive care unit(1 day)
  • Mortality(1 day)
  • number of patients with pulmonary complications(1 day)
  • Number of Participants with pulmonary stress and strain(1 day)

Study Sites (1)

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