esophageal achalasia
Conditions
Interventions
anesthesia induction with remimazolam
anesthesia induction with propofol
Sponsors
Showa University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) patients undergoing elective surgery for esophageal achalasia in Showa University Koto Toyosu Hospital 2) 20 to 50 years old 3) patients who have given their written informed consent to participate in the research
Exclusion criteria
Exclusion criteria: 1) allergy to benzodiazepine, propofol, inhalation anesthetics, or soybeans 2) history or family history of malignant hyperthermia 3) chronic intake of benzodiazepine 4) pregnancy 5) neurological disorders that may affect the electroencephalographic waveform 6) American Society of Anesthesiologist physical status 3 or above 7) patients who have been judged ineligible by the anesthesiologists in charge of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time from start of remimazolam or propofol administration to loss of consciousness | — |
Secondary
| Measure | Time frame |
|---|---|
| Time from start of remimazolam or propofol administration to respiratory arrest, dose of remimazolam or propofol for loss of consciousness, injection pain, time from start of remimazolam or propofol administration to completion of tracheal intubation, hemodynamics during anesthesia induction, and electroencephalographic change during anesthesia induscion | — |
Countries
Japan
Contacts
Public ContactDaiki Nagane
Showa University Koto Toyosu Hospital Anesthesiology
Outcome results
None listed