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Respiratory Function Monitoring of Mechanical Ventilation in Patients With Chest Blunt Injury

Respiratory Function Monitoring of Patients With Chest Blunt Injury With Mechanical Ventilation

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06386120
Enrollment
80
Registered
2024-04-26
Start date
2024-05-31
Completion date
2026-07-31
Last updated
2024-04-26

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

Conditions

Lung Contusion

Keywords

chest contusion, lung contusion, electrical impedance tomography, pulmonary perfusion

Brief summary

The goal of this observational study is to learn about EIT in observing the application of lung protective ventilation strategies in patients with pulmonary contusion, particularly the impact on pulmonary ventilation blood flow ratio, oxygen, and condition. The main question it aims to answer is: Can lung protective ventilation strategies improve respiratory function in patients with severe chest contusion? We will collect clinical data of participants who already taking lung protective ventilation strategies as part of their regular medical care.

Detailed description

Trauma is the leading cause of death among middle-aged and young people in China, with over 25% of patients dying from chest trauma. The incidence of pulmonary contusion in severe chest trauma is over 70%, and it is an important cause of respiratory failure and even death in patients. The occurrence of pulmonary contusion and respiratory failure in patients with chest contusion is a dynamic process, and Regional inhomogeneities of the damaged lung should be taken into consideration to develop improved ventilation strategies. Currently, there is no ideal monitoring method to evaluate the severity of injury, and guide the ventilation strategies. Electrical impedance tomography (EIT) is a non-invasive, radiation-free imaging technique. It measures regional lung ventilation and aeration distribution by means of changes in electrical potentials at the skin surface of the chest wall during breathing cycles, which has been proven to have good practicality in patients with non-invasive ARDS and pulmonary embolism. In this study, we aim to characterize the physiologic effects of positive end expiratory pressure (PEEP) on key mechanisms of regional lung protection, namely: recruitment, reduced atelectrauma, and improved ventilation-perfusion matching, by CT scan and EIT

Interventions

OTHERPEEP setting strategy

The attending physician selects different PEEP setting strategies

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with severe chest contusion admitted to the intensive care unit (ICU); * Abbreviated Injury Scale (AIS) ≥ 3 and/or Blunt Pulmonary Contusion 18 score (BPC18) ≥ 3; * Age range from 18 to 90 years old; * Mechanical ventilation; * Stay in the ICU for less than 12 hours.

Exclusion criteria

* Perinatal women; * Expected to be mechanically ventilated for less than 48 h; * Expected duration of stay in the ICU is less than 24 hours; * There are contraindications for the use of EIT (pacemaker implantation, local skin wounds after chest surgery, etc.); * Accept extracorporeal membrane oxygenator; * Mechanical ventilation\>7 days; * Confirmed ventilator-associated pneumonia; * Pneumothorax without drainage or presence of subcutaneous emphysema.

Design outcomes

Primary

MeasureTime frameDescription
ventilation blood flow ratiothrough study completion, an average of 1 yearventilation blood flow ratio of lung

Secondary

MeasureTime frameDescription
28-day mortalitythrough study completion, an average of 1 year28-day mortality
Mechanical ventilation-free from day 1 to 28through study completion, an average of 1 yearMechanical ventilation-free from day 1 to 28
oxygenation indexthrough study completion, an average of 1 yearoxygenation index of participant
Length of hospital staythrough study completion, an average of 1 yearLength of hospital stay
The rate of successful weaningthrough study completion, an average of 1 yearthe absence of the requirement for ventilatory support, without reintubation, a cardiac arrest event, or mortality within 48h after extubating or withdrawal
Length of ICU staythrough study completion, an average of 1 yearLength of ICU stay

Contacts

Primary ContactShu Li, doctor
lishu2401@163.com+86 010 88324480

Outcome results

None listed

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