Patients with oral valproate
Conditions
Interventions
None listed
Sponsors
Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Dental Anesthsiology and Special Care Dentistry
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Participants of the present study are patients who have the plan of a general anesthesia in Okayama university hospital.
Exclusion criteria
Exclusion criteria: Patients without consent of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The change of BIS index during anesthesia induction, the serum concentration of propofol after injection and the change of blood pressure and heart rate during anesthesia | — |
Countries
Japan
Contacts
Public ContactHitoshi Higuchi
Okayama University Hospital Dental Anesthesiology
Outcome results
None listed