UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037059
Receipt number R000042226
Scientific Title The hemodynamics of Labor in Women undergoing Vaginal Deliveries as determined by LIDCO rapid V3
Date of disclosure of the study information 2019/06/15
Last modified on 2021/11/30 15:10:36

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Basic information

Public title

The hemodynamics of Labor in Women undergoing Vaginal Deliveries as determined by LIDCO rapid V3

Acronym

The hemodynamics of Labor in Women undergoing Vaginal Deliveries as determined by LIDCO rapid V3

Scientific Title

The hemodynamics of Labor in Women undergoing Vaginal Deliveries as determined by LIDCO rapid V3

Scientific Title:Acronym

The hemodynamics of Labor in Women undergoing Vaginal Deliveries as determined by LIDCO rapid V3

Region

Japan


Condition

Condition

Hemodynamic changes during labor of healthy pregnant women

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Hemodynamic changes during delivery

Basic objectives2

Others

Basic objectives -Others

Cardiac output

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Hemodynamic changes during epidural delivery

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


Not applicable

Gender

Female

Key inclusion criteria

ASA1-2

Key exclusion criteria

The person in charge of research judged it to be inappropriate

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Maiko
Middle name
Last name Satomoto

Organization

Toho University

Division name

Anesthesiology

Zip code

1438541

Address

6-11-1, Omori-Nishi, Ota-ku, Tokyo 143-8541, Japan

TEL

0337624151

Email

maiko.satomoto@med.toho-u.ac.jp


Public contact

Name of contact person

1st name Maiko
Middle name
Last name Satomoto

Organization

Toho University

Division name

Research consultation desk

Zip code

1438541

Address

6-11-1, Omori-Nishi, Ota-ku, Tokyo 143-8541, Japan

TEL

0337624151

Homepage URL


Email

maiko.satomoto@med.toho-u.ac.jp


Sponsor or person

Institute

Toho University

Institute

Department

Personal name



Funding Source

Organization

Toho University, Department of Anesthesiology
Self Funding

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Toho University

Address

6-11-1, Omori-Nishi, Ota-ku, Tokyo 143-8541, Japan

Tel

0337624151

Email

omori.rinri@ext.toho-u.ac.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

2019 Year 06 Month 15 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

25

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

Completed

Date of protocol fixation

2018 Year 12 Month 01 Day

Date of IRB

2019 Year 02 Month 01 Day

Anticipated trial start date

2019 Year 06 Month 15 Day

Last follow-up date

2021 Year 12 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Analysis data (sample) protects personal information by deleting identifiable personal information (anonymization). In anonymization, random numbering is performed in Excel to create a correspondence table. Also, all information files are used with a password, and the stored USB and paper media information is also stored in a locker locker and not used on PCs that can connect to the Internet environment. Analysis data after the end of the study is stored by a research executor in a locker that takes 10 years.


Management information

Registered date

2019 Year 06 Month 13 Day

Last modified on

2021 Year 11 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042226