Patients undergoing non-cardiac surgery under general anesthesia
Conditions
Interventions
None listed
Sponsors
St. Marianna University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients aged 18 years or older. 2.Patients undergoing non-cardiac surgery under general anesthesia. 3.Patients scheduled for core body temperature monitoring (esophageal or bladder temperature) for 180 minutes or longer during general anesthesia. 4.Patients (or their legally acceptable representatives) who provide written informed
Exclusion criteria
Exclusion criteria: 1.Patients undergoing (or likely to undergo) surgery or procedures at the neck or inguinal region. 2.Patients with anatomical abnormalities, infections, or severe wounds on the skin of the neck or inguinal region. 3.Patients in surgical positions that prevent the attachment of temperature sensors to the neck or inguinal region. 4.Patients with a history of contact dermatitis or hypersensitivity to medical adhesive tapes. 5.Patients otherwise judged inappropriate for participation by the principal or sub-investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Differences in measured body temperature (absolute values and mean errors) between the sensor attached to the neck and the sensor attached to the inguinal region. * Differences in measured body temperature (absolute values and mean errors) between the sensor attached to the inguinal region and bladder/esophageal temperature. * Chronological changes in body temperature measured at the three distinct sites (inguinal region, neck, and bladder or esophagus). | — |
Countries
Japan
Contacts
Public ContactHIROTAKA OKUDA
Department of Anesthesiology, St. Marianna University School of Medicine Department of Anesthesiology
Outcome results
None listed