UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017817
Receipt number R000020573
Scientific Title A recent survey of postoperative nausea and vomiting
Date of disclosure of the study information 2015/06/08
Last modified on 2016/07/09 08:25:20

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Basic information

Public title

A recent survey of postoperative nausea and vomiting

Acronym

A recent survey of postoperative nausea and vomiting

Scientific Title

A recent survey of postoperative nausea and vomiting

Scientific Title:Acronym

A recent survey of postoperative nausea and vomiting

Region

Japan


Condition

Condition

Patients undergone operation

Classification by specialty

Anesthesiology Adult Child

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Prospective study of incidence of PONV

Basic objectives2

Others

Basic objectives -Others

Prospective study of risk factors for PONV

Trial characteristics_1

Exploratory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

The incidence of PONV in 24hr after operation

Key secondary outcomes

The risk factors for PONV


Base

Study type

Observational


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

0 days-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Every postoperative patient who have undergone a surgical procedure under anesthetic management by a anesthesiologist

Key exclusion criteria

Patients postoperatively managed with artificial ventilation, patients maintained with more than 2 kinds of anesthetic, patients underwent electricconvulsive therapy

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Maiko HOSHIKA

Organization

Nagoya City University Graduate School of Medical Sciences

Division name

Department of Anesthesiology and Intensive Care Medicine

Zip code


Address

1-Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, JAPAN

TEL

052-851-5511

Email

myconjar@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Maiko HOSHIKA

Organization

Nagoya City University Graduate School of Medical Sciences

Division name

Department of Anesthesiology and Intensive Care Medicine

Zip code


Address

1-Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, JAPAN

TEL

052-851-5511

Homepage URL


Email

myconjar@yahoo.co.jp


Sponsor or person

Institute

Nagoya City University Graduate School of Medical Sciences

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor

Nagoya city east medical center, Kainan hospital, Okazaki city hospital

Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

名古屋市東部医療センター(愛知県)、JA厚生連海南病院(愛知県)、岡崎市民病院(愛知県)


Other administrative information

Date of disclosure of the study information

2015 Year 06 Month 08 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

Preinitiation

Date of protocol fixation

2015 Year 06 Month 08 Day

Date of IRB


Anticipated trial start date

2015 Year 06 Month 08 Day

Last follow-up date

2015 Year 12 Month 31 Day

Date of closure to data entry

2016 Year 06 Month 16 Day

Date trial data considered complete

2016 Year 07 Month 09 Day

Date analysis concluded

2016 Year 08 Month 31 Day


Other

Other related information

Prospective study, Incidence of PONV and Risk for PONV, over 1000 cases


Management information

Registered date

2015 Year 06 Month 04 Day

Last modified on

2016 Year 07 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020573


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name