UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037013
Receipt number R000042165
Scientific Title The assessment of gastric antral cross-sectional area that increase aspiration risk by ultrasonography
Date of disclosure of the study information 2019/06/11
Last modified on 2022/06/13 20:55:41

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

The assessment of gastric antral cross-sectional area that increase aspiration risk by ultrasonography

Acronym

The assessment of gastric antral cross-sectional area that increase aspiration risk by ultrasonography

Scientific Title

The assessment of gastric antral cross-sectional area that increase aspiration risk by ultrasonography

Scientific Title:Acronym

The assessment of gastric antral cross-sectional area that increase aspiration risk by ultrasonography

Region

Japan


Condition

Condition

healthy

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to clarify the gastric antral cross-sectional area that increase aspiration risk in Japanese

Basic objectives2

Others

Basic objectives -Others

to help to assess preoperative aspiration risk

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

gastric antral cross-sectional area after intake 1.5ml/kg water

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

20 years-old <=

Age-upper limit

60 years-old >=

Gender

Male and Female

Key inclusion criteria

ASA-PS1 or 2

Key exclusion criteria

ASA-PS >2
pregnant women

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Gaku
Middle name
Last name Inagawa

Organization

Yokohama Municipal Citizen's Hospital

Division name

Anesthesiology

Zip code

240-8555

Address

56, Okazawacho, Hodogaya-ku, Yokohama-shi, Kanagawa, Japan

TEL

0453311961

Email

yokohama.city.anesth@gmail.com


Public contact

Name of contact person

1st name Misaki
Middle name
Last name Goto

Organization

Yokohama Municipal Citizen's Hospital

Division name

Anesthesiology

Zip code

240-8555

Address

56, Okazawacho, Hodogaya-ku, Yokohama-shi, Kanagawa, Japan

TEL

045-331-1961

Homepage URL


Email

yokohama.city.anesth@gmail.com


Sponsor or person

Institute

Yokohama Municipal Citizen's Hospital

Institute

Department

Personal name



Funding Source

Organization

none

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

Yokohama Municipal Citizen's Hospital Ethics Committie

Address

56, Okazawacho, Hodogaya-ku, Yokohama-shi, Kanagawa, 240-8555 Japan

Tel

045-331-1961

Email

by-sh-shomu@city.yokohama.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

横浜市立市民病院(神奈川県)


Other administrative information

Date of disclosure of the study information

2019 Year 06 Month 11 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

50

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

2019 Year 05 Month 01 Day

Date of IRB

2019 Year 05 Month 17 Day

Anticipated trial start date

2019 Year 06 Month 11 Day

Last follow-up date

2020 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

1. measuring gastric antral cross-sectional area by ultrasonography after fastened 8 hours and after intake 1.5ml/kg water that is amount seemed to increase aspiration risk

2. to determine between the preoperative aspiration risk and gastric antral cross-sectional area


Management information

Registered date

2019 Year 06 Month 10 Day

Last modified on

2022 Year 06 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042165


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name