Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
ID06790875

Effects of Low Tidal Volume and Airway Pressure Release Ventilation on Lung Tissue Mechanics in ARDS Patients Under Mechanical Ventilation: A Prospective Randomized Crossover Study

Led by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Updated on 2025-01-24

15

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how two types of mechanical ventilation, low tidal volume ventilation (LTV) and airway pressure release ventilation (APRV), affect lung tissue mechanics in adults with Acute Respiratory Distress Syndrome (ARDS). The main goal is to determine which ventilation method better improves lung function and patient safety during mechanical ventilation. This prospective randomized crossover study is led by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology. Participants will receive either APRV or LTV during the trial. In the APRV group, mechanical ventilation involves setting a high pressure based on the plateau pressure from LTV, with specific timing to maintain lung recruitment and optimize airflow. The study compares these two ventilation modes to observe their effects on lung tissue mechanics and respiratory function in ARDS patients. During the study, researchers will measure dynamic relative regional lung strain (DRRS), mechanical power, platform pressure, and mean airway pressure over a maximum of 4 hours. Participants will be closely monitored to evaluate how each ventilation method influences lung mechanics. The trial includes adults aged 18 to 80 years who meet specific ARDS criteria and are under invasive mechanical ventilation. Consent from patients or family members is required for participation.

CONDITIONS

Brief Title

Effects of Low Tidal Volume and Airway Pressure Release Ventilation on Lung Tissue Mechanics in ARDS Patients Under Mechanical Ventilation: A Prospective Randomized Crossover Study

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meets the diagnostic criteria of the 2023 Global New Definition of ARDS.
  • Age between 18 and 80 years.
  • PaO2/FiO2 ratio less than or equal to 200.
  • Within 12 hours of starting invasive mechanical ventilation treatment.
  • Consent obtained from patient or family and signed informed consent form.
Not Eligible

You will not qualify if you...

  • Age younger than 18 years or older than 80 years.
  • Uncorrected shock of any type.
  • Chronic obstructive pulmonary disease (COPD), pulmonary embolism, right heart failure, pulmonary hypertension, or severe arrhythmia.
  • Contraindications for Electrical Impedance Tomography such as extensive chest skin damage, infection, pacemaker implantation, implanted automatic defibrillator, pneumothorax, mediastinal emphysema, or large pleural effusion.
  • Pregnant or breastfeeding women.
  • Patients planned for ECMO treatment.
  • Current or previous participation in other clinical studies.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - Up to 4 hours

Participants receive airway pressure release ventilation (APRV) or low tidal volume ventilation as part of mechanical ventilation to evaluate lung tissue mechanics.

1 intervention period lasting up to 4 hours

Trial Site Locations

Total: 1 location

1

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China

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Research Team

X

Xiaojing Zou Professor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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