Patients undergoing general anesthesia for robot-assisted laparoscopic surgery
Conditions
Interventions
Continuous measurement of esophageal pressure with the insertion of an esophageal pressure measuring balloon device
Sponsors
The University of Tokyo Hospital
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1 Patients scheduled for robot-assisted laparoscopic surgery 2 Patients scheduled to use a cuffed endotracheal intubation tube 3 Patients who have been fully informed of the study, fully understood, and have given their voluntary written consent to participate in the study
Exclusion criteria
Exclusion criteria: 1 Patients with known esophageal disease or known history of esophageal disease 2 Patients with a past history of upper gastrointestinal surgery 3 Patients with suspected abnormalities in the laryngeal trachea anatomy such as previous tracheostomy, airway stenosis, or tracheomalacia 4 Patients with potential complications with intralesional pressure balloon placement such as uncontrolled coagulation abnormalities, severe thrombocytopenia, nasal involvement, or esophageal varices 5 As determined by the Minister of Health, Labour and Welfare, patients evaluated as difficult to anesthetize in their pre-anesthetic state 6 Other patients who are deemed unsuitable as subjects by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between esophageal pressure and other respiratory parameters | — |
Secondary
| Measure | Time frame |
|---|---|
| Subgroup analysis for correlation contributions | — |
Countries
Japan
Contacts
Public ContactYoko Hoshino
The University of Tokyo Hospital Anesthesiology and pain relief center
Outcome results
None listed