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Clinical study on the effect of body position change on SBT in ARDS patients under EIT and diaphragmatic ultrasound monitoring

Clinical study on the effect of body position change on SBT in ARDS patients under EIT and diaphragmatic ultrasound monitoring

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104392
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-06-20
Completion date
Unknown
Last updated
2025-06-24

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

Conventional group:Supine position during SBT
Semi-recumbent group:Semi-recumbent position during SBT
Sitting group:Sitting position during SBT

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. ARDS patients with mechanical ventilation whose condition has been relieved or improved; 2. The patient is awake and has the effort of self-inspiration; 3. Sao 2 > 90%, FiO2=5mL/kg, no obvious acidosis; 5. Hemodynamic stability, systolic blood pressure of 90-160mmHg, no vasoactive drugs or low-dose pressor (dobutamine < 5 µ g/kg/min or norepinephrine < 0.15 µ g/kg/min), and heart rate <=140 beats/min; 6. No fever, anemia, good mental state, etc.

Exclusion criteria

Exclusion criteria: 1. Age < 18 years old; 2. Pregnancy and severe obesity; 3. There are contraindications for EIT such as rib fracture, chest and hand; 4. ICU stay time <=48 hours.

Design outcomes

Primary

MeasureTime frame
Ventilation blood flow ratio;Shunt rate;Dead space rate;Region of interest;

Secondary

MeasureTime frame
Plateau pressure;Lung compliance;Diaphragm activity;Diaphragmatic thickening fraction;

Countries

China

Contacts

Public ContactRuyang Xiong; Zheng Junbo

The Second Affiliated Hospital of Harbin Medical University

xiongruyang@hrbmu.edu.cn+86 188 4575 2373

Outcome results

None listed

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