Postoperative nausea and vomiting
Conditions
Interventions
None listed
Sponsors
Kagawa University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Recruitment will take place at the researcher's affiliated institution between the date of approval by the ethics committee and March 31, 2028, targeting healthy adult volunteers who are willing to participate. Participants must meet all of the inclusion criteria and must not fall under any of the exclusion criteria. Eligible participants are healthy adult volunteers aged 20 years or older who have provided written informed consent to participate in this study.
Exclusion criteria
Exclusion criteria: Volunteers with severe systemic complications, such as heart failure, renal failure, liver failure, or respiratory failure. Volunteers with severe mental disorders or associated psychiatric symptoms. Volunteers with a history of claustrophobia or nyctophobia. Volunteers with metal implants in their bodies. Pregnant women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of fMRI and sMRI Data Obtained Using a 3T GE SIGNA Architect at Kagawa University Hospital MRI Facility, with and without Neiguan (PC6) Stimulation | — |
Secondary
| Measure | Time frame |
|---|---|
| Analysis of the Correlation Between fMRI and sMRI Responses to Neiguan (P6) Stimulation and Apfel Score | — |
Countries
Japan
Contacts
Public ContactSHIRAISHI REN
Kagawa University Hospital Department of Anesthesiology and pain management clinic
Outcome results
None listed