Upper airway obstruction Upper airway obstruction
Conditions
Interventions
Intervention group: Perform sedation adjustment with reference to the data from the type 3 portable sleep apnea monitor.
Non-intervention group: Perform sedation adjustment without reference to the da
Sponsors
Masuda Rikuo
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1) Patients undergoing dental treatment under intravenous sedation. 2) Male over 20 years old 3) BMI, over 18.5 under 25 4) Patients whose preliminary sleep test result was less than AHI 10.0 times / hr 5) Patients who are healthy, or have mild systemic disease 6) Patients who agree to participate in this study
Exclusion criteria
Exclusion criteria: 1) Patients who are not indicated for IVS 2) Patients who have congnitive and sensor impairment 3) Patients who judged to be ineligible fot this study by the doctor 4) Patients who don't agree to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abnormal Breathing Index (Apnea): ABI-A | — |
Secondary
| Measure | Time frame |
|---|---|
| Data from type 3 portable sleep apnea monitor, resurt of sleep study and questionnaire, medical informations, resurt of EEG recording and vital signs recording, anesthesia records, data from various monitors | — |
Contacts
Public ContactAkiko Nishimura
Showa Medical University Hospital
Outcome results
None listed