Anesthesia, Spinal Clinical Trial
Official title:
Comparison of the Upper Airway Patency by Dexmedetomidine and Propofol Used for Sedation
Verified date | September 2017 |
Source | Seoul National University Bundang Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Under the hypothesis that dexmedetomidine sedation would result in less upper airway obstruction, we evaluated the occurrence of upper airway collapse or the requirement of airway intervention in patients with obstructive sleep apnea during dexmedetomidine or propofol sedation.
Status | Completed |
Enrollment | 52 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Surgery under spinal anesthesia - Intraoperative sedation - American Society of Anesthesiology physical status 1 or 2 - Apnea/hypopnea index 5-14/h in Watch-PAT 200 analysis Exclusion Criteria: - Anatomical defects on upper respiratory tract - Psychotic disorder - Drug addition - Alcohol addition - body mass index = 35 kg/m2 |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Bundang Hospital | Seongnam | Gyeonggi |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Bundang Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The occurrence of upper airway obstruction | When end-tidal carbon dioxide was not detected in spite of the respiratory effort during the sedation period, the case will be regarded as the occurrence of upper airway obstruction. | During the sedation period, an average of 3 hours. |
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