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Recruiting NCT06919484

The Physiological Effect of RCexp on Ventilation/Perfusion Distribution

Observational Acute Respiratory Distress Syndrome Mechanical Ventilation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: RCexp.
Who it may be relevant to
Registry conditions: Acute Respiratory Distress Syndrome, Mechanical Ventilation. Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Physiological Effect of RCexp on Ventilation/Perfusion Distribution in Patients With ARDS

Overview

With the exception of setting the positive end-expiratory pressure (PEEP), the expiratory phase is commonly overlooked during MV. The expiratory time constant (RCexp) plays an important role in understanding the mechanical properties of the respiratory system in patients receiving mechanical ventilation. However, it is unclear that the effect of expiratory time constant on the ventilation and perfusion distribution.

Detailed description

With the exception of setting the positive end-expiratory pressure (PEEP), the expiratory phase is commonly overlooked during MV. The expiratory time constant (RCexp) plays an important role in understanding the mechanical properties of the respiratory system in patients receiving mechanical ventilation. However, it is unclear that the effect of expiratory time constant on the ventilation and perfusion distribution.

Interventions

  • Other RCexp
    patients received different RCexp

Primary outcome measures

  • Difference in ventilation/perfusion mismatch [Time frame: 4 hours]
Secondary outcome measures (2)
  • Difference in dead space [Time frame: 4 hours]
  • Difference in shunt [Time frame: 4 hours]

Eligibility criteria

Inclusion criteria

adult patients with ARDS receiving mechanical ventilation no more than 72 hours

Exclusion criteria

  • age <18 years old
  • patient undergoing legal protection
  • contra-indications to EIT (e. g. severe chest trauma or wounds)
  • pneumothorax
  • patient undergoing ECMO
  • pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-crossover

Study locations

China · 1 center
  • Zhongda Hospital, School of Medicine, Southeast University — Nanjing

Identifiers

NCT: NCT06919484 · RCexp_ventilation/perfusion

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗