Desflurane compared with sevoflurane on awakeing and quality of recovery in gynecological sugery: a randomized, double-blinded controlled trial

Desflurane compared with sevoflurane on awakeing and quality of recovery in gynecological sugery: a randomized, double-blinded controlled trial - Desflurane compared with sevoflurane on awakeing and quality of recovery in gynecological sugery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000028151

Enrollment

Registered

2017-07-10

Start date

2017-04-01

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

cervical polyps myoma of the uterus

Interventions

During operations, anesthesia maintenance was achieved using 3% desflurane for cases . At the end of operations, the anesthetic agent is discontinued. During operations, anesthesia maintenance was ach

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: study-eligible subjects are ASA PS 1 or 2 women undergoing trans cervical resection (TCR).

Exclusion criteria

Exclusion criteria: obese patients whose BMI is 30 or more, or subjects taking central nervous system depressants

Design outcomes

Primary

Measure	Time frame
time to awaking from discontinuation of anesthesia	—

Secondary

Measure	Time frame
post anesthetic complications	—

Countries

Japan

Contacts

Public ContactSuguru Yamamoto

Ohkubo hospital department of anesthesiology

suguru-.-yamamoto@hotmail.co.jp03-5273-7711

Outcome results

None listed

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