UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020689
Receipt number R000023873
Scientific Title Perioperative risk factors for postoperative nausea and vomiting
Date of disclosure of the study information 2016/01/31
Last modified on 2017/07/25 17:05:56

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Basic information

Public title

Perioperative risk factors for postoperative nausea and vomiting

Acronym

Perioperative risk factors for postoperative nausea and vomiting

Scientific Title

Perioperative risk factors for postoperative nausea and vomiting

Scientific Title:Acronym

Perioperative risk factors for postoperative nausea and vomiting

Region

Japan


Condition

Condition

postoperative nausea and vomiting

Classification by specialty

Surgery in general Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate how perioperative risk factors influence postoperative nausea and vomiting

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Postoperative nausea and vomiting

Key secondary outcomes



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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who underwent general anesthesia in Osaka City University Hospital from 2009 to 2015

Key exclusion criteria

Patients who were intubated before surgery, who underwent tracheostomy after surgery, or who underwent esophagectomy

Target sample size

14240


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Katsuaki Tanaka

Organization

Osaka City University Graduate School of Medicine

Division name

Anesthesiology

Zip code


Address

1-5-7, Asahimachi, Abeno-ku, Osaka 545-8585 Japan

TEL

06-6645-2186

Email

anesth@med.osaka-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takashi Juri

Organization

Osaka City University Graduate School of Medicine

Division name

Anesthesiology

Zip code


Address

1-5-7, Asahimachi, Abeno-ku, Osaka 545-8585 Japan

TEL

06-6645-2186

Homepage URL


Email

anesth@med.osaka-cu.ac.jp


Sponsor or person

Institute

Osaka City University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Osaka City University Graduate School of Medicine

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


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



Other administrative information

Date of disclosure of the study information

2016 Year 01 Month 31 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

No longer recruiting

Date of protocol fixation

2015 Year 12 Month 31 Day

Date of IRB


Anticipated trial start date

2016 Year 01 Month 31 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

We collect data related to postoperative nausea and vomiting from perioperative records of patients who underwent general anesthesia.We also collect information about age,sex,operative time,drugs,operation method and position,which may exert influence over postoperative nausea and vomiting. Thereafter,multiple logistic regression analysis are performed using them.


Management information

Registered date

2016 Year 01 Month 21 Day

Last modified on

2017 Year 07 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023873


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name