UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022759
Receipt number R000026218
Scientific Title Comparison of the incidence of PONV in Desflurane Versus Sevoflurane Anesthesia (Including cases of hydroxyzine administered as antiemetic)
Date of disclosure of the study information 2016/06/17
Last modified on 2021/05/21 15:36:16

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Basic information

Public title

Comparison of the incidence of PONV in Desflurane Versus Sevoflurane Anesthesia (Including cases of hydroxyzine administered as antiemetic)

Acronym

Comparison of the incidence of PONV in Desflurane Versus Sevoflurane Anesthesia

Scientific Title

Comparison of the incidence of PONV in Desflurane Versus Sevoflurane Anesthesia (Including cases of hydroxyzine administered as antiemetic)

Scientific Title:Acronym

Comparison of the incidence of PONV in Desflurane Versus Sevoflurane Anesthesia

Region

Japan


Condition

Condition

Patients with surgery under general anethsesia

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

In this study, we performed meta-analysis comparing of the incidence of PONV in Desflurane Versus Sevoflurane at hydroxyzine administration example or non-administration example.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The presence or absence of nausea and vomiting

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

16 years-old <=

Age-upper limit

70 years-old >

Gender

Male and Female

Key inclusion criteria

Patients undergoing general anesthesia with desflurane or sevoflurane

Key exclusion criteria

Patients receiving opioids after surgery

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Takashi
Middle name
Last name Kono

Organization

Toyooka Public Hospital

Division name

Department of Anesthesiology

Zip code

668-8501

Address

1094 Tobera Toyooka City, Hyogo, Japan

TEL

0796-22-6111

Email

konotori-konotori@gaia.eonet.ne.jp


Public contact

Name of contact person

1st name Takashi
Middle name
Last name Kono

Organization

Toyooka public hospital

Division name

Department of Anesthesiology

Zip code

668-8501

Address

1094 Tobera Toyooka City, Hyogo, Japan

TEL

0796-22-6111

Homepage URL


Email

konotori-konotori@gaia.eonet.ne.jp


Sponsor or person

Institute

Toyooka Public Hospital

Institute

Department

Personal name



Funding Source

Organization

Toyooka Public Hospital

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Toyooka public hospital

Address

1094 Tobera Toyooka City, Hyogo, Japan

Tel

0796-22-6111

Email

konotori-konotori@gaia.eonet.ne.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2016 Year 06 Month 17 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Open public recruiting

Date of protocol fixation

2016 Year 01 Month 04 Day

Date of IRB

2016 Year 02 Month 03 Day

Anticipated trial start date

2016 Year 03 Month 01 Day

Last follow-up date

2022 Year 06 Month 17 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

nothing


Management information

Registered date

2016 Year 06 Month 15 Day

Last modified on

2021 Year 05 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026218


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name