UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010223
Receipt number R000011859
Scientific Title Prediction of hypotension during spinal anesthesia for caesarean section: a observational study.
Date of disclosure of the study information 2013/03/15
Last modified on 2015/03/19 18:20:51

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Basic information

Public title

Prediction of hypotension during spinal anesthesia for caesarean section: a observational study.

Acronym

Prediction of hypotension during spinal anesthesia for caesarean section: a observational study.

Scientific Title

Prediction of hypotension during spinal anesthesia for caesarean section: a observational study.

Scientific Title:Acronym

Prediction of hypotension during spinal anesthesia for caesarean section: a observational study.

Region

Japan


Condition

Condition

Women who were to undergo elective cesarean delivery under spinal anesthesia.

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Test the ability of pre-anesthesia Pleth Variability Index (PVI) to predict hypotension after spinal anesthesia during cesarean section.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Estimate Receiver operating characteristic (ROC) curve, and sensitivity and specificity.

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

Women who were to undergo elective cesarean delivery under spinal anesthesia.

Key exclusion criteria

Hypertension
Diabetes
Preanesthetic Cardiovascular events
Arrhythmia
Preeclampsia
Placenta previa
Multiple pregnancy

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Masashi Yokose

Organization

Yokohama city university school of medicine

Division name

Department of anesthesiology

Zip code


Address

3-9 Fukuura, Kanazawa-ku, Yokohama, JAPAN

TEL

0810457872918

Email

yokose_p12@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Masashi Yokose

Organization

Yokohama city university school of medicine

Division name

Department of anesthesiology

Zip code


Address

3-9 Fukuura, Kanazawa-ku, Yokohama, JAPAN

TEL

0810457872918

Homepage URL


Email

yokose_p12@yahoo.co.jp


Sponsor or person

Institute

Yokohama city university school of medicine department of anesthesiology

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


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

2013 Year 03 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


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

2011 Year 10 Month 01 Day

Date of IRB


Anticipated trial start date

2011 Year 10 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The aim of this prospective observational study was to test the ability of pre-anesthesia PVI to predict hypotension after spinal anesthesia for caesarean section.


Management information

Registered date

2013 Year 03 Month 12 Day

Last modified on

2015 Year 03 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011859


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name