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Desflurane compared with sevoflurane on quality of recovery and satisfaction in ambulatory anesthesia using laryngeal mask: randomized double-blinded controlled trial

Desflurane compared with sevoflurane on quality of recovery and satisfaction in ambulatory anesthesia using laryngeal mask: randomized double-blinded controlled trial - Desflurane compared with sevoflurane on quality of recovery and satisfaction

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019800
Enrollment
161
Registered
2016-04-01
Start date
2014-12-01
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

Healty Rhinitis or sinusitis patients

Interventions

Until discharge from hospitalization (about 8 hours) Desflurane4~5% Until discharge from hospitalization (about 8 hours) Sevofluran1%

Sponsors

Anestmedical Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: age:18~60y.o. male, female ASAPS1~2

Exclusion criteria

Exclusion criteria: ASAPS3~5

Design outcomes

Primary

MeasureTime frame
Time until to eat We will be evaluated until hospital discharge

Secondary

MeasureTime frame
time until to walk, time until to drink, patient satisfaction

Countries

Japan

Contacts

Public ContactKunitomo Kashiwagi

Anestmedical Co., Ltd. Ansthesiology

kunitomo19790406@yahoo.co.jp0473803954

Outcome results

None listed

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