Patient satisfaction and abnormal respiratory events during dental sedation.

Not Applicable

Recruiting

• Conditions: pper airway obstruction; Upper airway obstruction

• Registration Number: JPRN-jRCT1030220166
• Lead Sponsor: Kohzuka Yuuya

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-06-25
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

1) Patients undergoing dental treatment under intravenous sedation.
2) Over 20 years old
3) Patients who agree to participate in this study

Exclusion Criteria

1) Patients who are not indicated for intravenous sedation
2) Patients who were judged to be ineligible for this study by the doctor
3) Patients who don't agree to participate in this study

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Abnormal Breathing Index (Apnea): ABI-A

Secondary Outcome Measures

Name	Time	Method
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