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Study of the effect of intranasal pressure measurement on intravenous sedatio

Not Applicable
Recruiting
Conditions
pper airway obstruction
Upper airway obstruction
Registration Number
JPRN-jRCTs032210050
Lead Sponsor
Kohzuka Yuuya
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
52
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

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Abnormal Breathing Index (Apnea): ABI-A
Secondary Outcome Measures
NameTimeMethod
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
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