Analysis of incidence of postoperative nausea and vomiting after oral surgery with desflurane

Analysis of incidence of postoperative nausea and vomiting after oral surgery with desflurane - Analysis of incidence of postoperative nausea and vomiting after oral surgery with desflurane

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000011466

Enrollment

200

Registered

2013-08-19

Start date

2013-08-19

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients undergoing oral surgery with general anesthesia

Interventions

inhalation of 4-5% desflurane during general anesthesia inhalation of 1-2% sevoflurane during general anesthesia

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients who are American Society of Anesthesiologists Physical Status 1 or 2 and scheduled for operation required approximately 1-2 hours under general anesthesia

Exclusion criteria

Exclusion criteria: patients with ischemic heart disease patients with hepatic or renal dysfunction patients with histry of or family histry of malignant hyperthermia contraindication for propofol,sevoflurane and deslurane

Design outcomes

Primary

Measure	Time frame
Incidence of postoperative nausea and vomiting within 24 hours after operation	—

Secondary

Measure	Time frame
Time to extubation from end of operation, time to emergence from the anesthetic dosage end and time to recovering orientation from emergence	—

Countries

Japan

Contacts

Public ContactAiji Boku

Osaka University Graduate School of Dentistry Department of Dental Anesthsiology

bokuaiji@dent.osaka-u.ac.jp06-6879-2972

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026