Examination of aroma inhalation effect on post oral surgery nausea

Not Applicable

Recruiting

• Conditions: Postoperative nausea

• Registration Number: JPRN-jRCTs011210021
• Lead Sponsor: Kamekura Nobuhito

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-07-16
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 182

Inclusion Criteria

1. Patients scheduled to undergo oral surgery under general anesthesia at Surgical Center or Center for Oral Surgery of Hokkaido University Hospital
2. Age 20+
3. ASA physical status class 1 or 2
4. Written informed consent

Exclusion Criteria

1. Lack of judgment, such as intellectual disability
2. Allergy to the aroma essential oil
3. Olfactory disorder
4. Hemorrhagic diathesis
5. ICU management after general anesthesia
6. Scheduled to administer intraoperative antiemetic prophylaxis
7. Judged by the primary sponser to be inappropriate as research subjects

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Amount of change in the severity of nausea with and without aroma essential oil at the time of postoperative nausea.

Secondary Outcome Measures

Name	Time	Method
Antiemetics use rate, drug name and dose used, patient satisfaction, adverse events.