Skip to content

Research on patient-ventilator asynchrony based on flexible wearable respiratory monitoring system

Research on patient-ventilator asynchrony based on flexible wearable respiratory monitoring system

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093126
Enrollment
Unknown
Registered
2024-11-28
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

lung injury

Interventions

Gold Standard:Manual monitoring + esophageal pressure and/or electromyographic monitoring of the diaphragm through the esophageal tube
Index test:Mechanical power equivalent model Patient-ventilator asynchrony diagnostic model Risk prediction model for weaning risk

Sponsors

West China Tianfu Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Selection criteria for normal volunteers: (1) Age >= 18 years old, gender not limited; (2) There is no weight limit. At the time of enrollment, according to the BMI body mass index, it is divided into: lean, BMI index30; (3) Normal cardiopulmonary function (FEV1/FVC>70%, and FEV160cmH2O) (5) The body's motor function is sound; (6) No history of neurological and respiratory diseases; (7) Sign the informed consent form and be willing to participate in the trial. Inclusion criteria for ICU patients: (1) Age >= 18 years old, gender not limited; (2) There is no weight limit. At the time of enrollment, subgroups were divided based on BMI: lean, BMI30; (3) Invasive mechanical ventilation status (mechanical ventilation through tracheal intubation or tracheotomy); According to the respiratory ventilation mode, subgroups are divided into low tidal volume ventilation and non low tidal volume ventilation. (4) The authorized person/patient signs an informed consent form and is willing to participate in the trial.

Exclusion criteria

Exclusion criteria: Exclusion criteria for normal volunteers: (1) Pregnancy status; (2) Chest deformity. Exclusion criteria for ICU patients: (1) Pregnancy status; (2) Plan to withdraw the aircraft within 24 hours; (3) Severe respiratory center depression, high paraplegia, and neuromuscular disorders; (4) Esophageal obstruction, esophageal perforation, severe esophageal variceal bleeding, esophageal, gastric or lung surgery, diaphragmatic hernia, thoracic deformity; (5) Bronchopleural fistula, pneumothorax, mediastinal emphysema, thoracic drainage.

Design outcomes

Primary

MeasureTime frame
Patient-ventilator asynchrony;

Secondary

MeasureTime frame
Sensitivity ;Specificity;

Countries

China

Contacts

Public ContactYan Kang

West China Tianfu Hospital of Sichuan University

kangyan@scu.edu.cn+86 189 8086 1566

Outcome results

None listed

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