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The effect of APRV and LTV on respiratory function in patients with different types of ARDS: a single-center, randomized controlled study

The effect of APRV and LTV on respiratory function in patients with different types of ARDS: a single-center, randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043657
Enrollment
Unknown
Registered
2021-02-24
Start date
2021-03-02
Completion date
Unknown
Last updated
2021-06-22

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

Conditions

Acute respiratory distress syndrome

Interventions

airway pressure release ventilation:airway pressure release ventilation
Low tidal volume protective ventilation:Low tidal volume protective ventilation

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the 2012 Berlin ARDS diagnostic criteria; 2. Oxygenation index <= 250mmHg under invasive mechanical ventilation; 3. Tracheal intubation and mechanical ventilation time < 48h at the time of inclusion; 4. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Age less than 18 years old or more than 80 years old; 2. BMI >= 35kg/m2 in patients with obesity; 3. Pregnant and breast-feeding women; 4. The expected time of invasive mechanical ventilation is less than 48h; 5. Neuromuscular diseases that are known to require prolonged mechanical ventilation treatment; 6. Severe chronic obstructive pulmonary disease; 7. Intracranial hypertension; 8. Lung bullae or pneumothorax, subcutaneous emphysema, mediastinal emphysema; 9. ECMO treatment has been performed when entering the ICU; 10. Refractory shock; 11. Severe cardiac dysfunction (New York Heart Association grade III or IV, acute coronary syndrome or persistent ventricular tachyarrhythmia), right heart enlargement, cardiogenic shock or after major cardiac surgery; 12. Not signed informed consent.

Design outcomes

Primary

MeasureTime frame
28 days without mechanical ventilation;

Secondary

MeasureTime frame
Days of mechanical ventilation;ICU hospitalization days;Died during ICU stay;Successful extubation;the number of days in hospital;Death during hospitalization;All-cause death 28 days after randomization;Drive pressure;Lung compliance;Platform pressure;Oxygenation index;Diaphragm activity;Diaphragm thickness;Time integral of blood flow rate of left ventricular outflow tract;Tricuspid annulus systolic displacement;Tricuspid regurgitation;Cytokines;cytology;

Countries

China

Contacts

Public ContactXiaojing Zou

Institute of Anesthesia and Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

249126734@qq.com+86 13995518630

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026