NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000023647

Registered date:16/08/2016

Which provides better postoperative recovery in combined general/epidural anesthesia? Sefofulurane/propofol coadministration vs propofol: a randomized clinical trial.

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedgynecology
Date of first enrollment2016/08/16
Target sample size70
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Sevoflurane/propofol coadministration anesthesial propofol anesthesia

Outcome(s)

Primary Outcomeincidence of postoperative nausea and vomitting
Secondary OutcomeAwaking time, cough score, emergence agitation score, incidence of postoperative nausea and vomittingQoL recovery score

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximum65years-old
GenderFemale
Include criteria
Exclude criteriacognitive impairment, Migrating to abdominal surgery, history of malignant hyperthermia, pregnant, invalid case of epidural anesthesia, questionnaire cannot be collected

Related Information

Contact

public contact
Name Uchinami Yuka
Address 33-2 Honcho Hakodate Hokkaido Japan Japan
Telephone 0138-52-1231
E-mail yukauma923@gmail.com
Affiliation Hakodate central general hospital anesthesiology
scientific contact
Name Yuka Uchinami
Address 33-2 Honcho Hakodate Hokkaido Japan Japan
Telephone 0138-52-1231
E-mail yukauma923@gmail.com
Affiliation Hakodate central general hospital anesthesiology