None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Men and women greater than 18 years old (inclusive); 2) Patients scheduled for gas pressure measurements with balloon catheters; 3) Subjects/their legal guardians who can understand and are willing to follow relevant requirements for the clinical trial agree to sign the ICF. 4) Patients scheduled for mechanically ventilation.
Exclusion criteria
Exclusion criteria: 1) Patients with unstable vital signs; 2) Respiratory obstruction of different causes; 3) Concomitant contraindications for gastrointestinal pressure measurement; 4) Pregnant or lactating women; 5) Subjects combined with other disorders that may affect the scientific integrity of data in this study; 6) Subjects who have received other test drugs or medical devices within 30 days prior to enrollment or 5 half-lives of the test drug, whichever is longer, or who are concurrently participating in the clinical studies of other drugs or medical devices; 7) Other conditions, in the investigator’s judgment, deemed inappropriate for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Consistence of measurement for Airway Pressure;Consistence of measurement for Esophageal pressure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Consistence of measurement for Gastric pressure;Consistence of measurement for Ptp; | — |
Countries
China
Contacts
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine