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NCT Number: NCT05098717

End-expiratory Trans-pulmonary Pressure Guided PEEP Titration in Patients With Pulmonary Fibrosis and UIP Pattern Undergoing Mechanical Ventilation

Patients with pulmonary fibrosis and associated usual interstitial pneumonia that require mechanical ventilation for acute respiratory failure experience poor clinical outcomes. This may be influenced by the unfavorable interaction between the fibrotic lung and the stress and strain stimuli generated during controlled ventilation. Although there is no consensus on how to ventilate these patients, much of the recommendations followed in clinical practice are taken from the experience on patients with acute respiratory distress syndrome. Among these, measuring the esophageal pressures and adjusting positive-end expiatory pressure to make trans-pulmonary pressures positive can decrease atelectasis, derecruitment of lung, and cyclical opening and closing of airways and alveoli, thus optimizing lung mechanics and oxygenation. The effect of this strategy on the fibrotic lung has not yet been documented. With this observational study we aim at documenting the effect of PEEP titration maneuver based on end-expiratory trans-pulmonary pressure on lung mechanics of patients with pulmonary fibrosis and UIP pattern,

Recruiting

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Azienda Ospedaliero Universitaria Policlinico di Modena

Modena, Italy

Location status: Recruiting

Location contact

Roberto Tonelli

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • pulmonary fibrosis with UIP pattern
  • subjected to endotracheal intubation and controlled mechanical ventilation for acute respiratory failure
  • candidate to a trial of PEEP titration according to positive end expiratory pressure.

Exclusion criteria

  • chest wall deformities
  • chronic obstructive pulmonary disease

Treatment and study plan

Primary outcomes

  1. Lung elastance

    Time frame: 2 hours.

    The effect of PEEP titration according to end-expiratory transpulmonary pressure on lung elastance will be analyzed.

Secondary outcomes

  1. P/F ratio

    Time frame: 2 hours

    The effect of PEEP titration according to end-expiratory transpulmonary pressure on P/F ratio will be analyzed.

Study contacts

Contact information is provided by the study sponsor or research team.

Roberto Tonelli

CONTACT

[email protected]

0039 0594225934

Sponsors and collaborators

Lead sponsor

University of Modena and Reggio Emilia

Other

Registry information

Acronym: ETROPON

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Oct 28, 2021
Registry last updated
Apr 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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