UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017394
Receipt number R000020000
Scientific Title Effect of vasopressors on plasma volume expansion effect of plasma substitutes
Date of disclosure of the study information 2015/06/02
Last modified on 2016/11/02 07:26:43

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Basic information

Public title

Effect of vasopressors on plasma volume expansion effect of plasma substitutes

Acronym

Vasopressors and plasma volume expansion effect

Scientific Title

Effect of vasopressors on plasma volume expansion effect of plasma substitutes

Scientific Title:Acronym

Vasopressors and plasma volume expansion effect

Region

Japan


Condition

Condition

Gastrointestinal surgery

Classification by specialty

Gastrointestinal surgery Anesthesiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To investigate whether continuous infsuion of vasopressors for hypotension during anesthesia induction increases volume expansion effect of plasma substituts

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Plasma volume expansion effect

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Continuous infusion of phenylephrine

Interventions/Control_2

Continuous infusion of saline

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

80 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients undergoing elective gastrointestinal surgery

Key exclusion criteria

Low cardiac, pulmonary or renal function

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tsuneo Tatara

Organization

Hyogo College of Medicine

Division name

Department of Anesthesiology and Pain Medicine

Zip code


Address

1-1 Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan

TEL

0798-45-6392

Email

ttatara@hyo-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Ethics Review Board of Hyogo College of Medicine

Organization

Hyogo College of Medicine

Division name

Ethics Review Board of Hyogo College of Medicine

Zip code


Address

1-1 Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan

TEL

0798-45-6164

Homepage URL


Email

rinri@hyo-med.ac.jp


Sponsor or person

Institute

Ethics Review Board of Hyogo College of Medicine

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


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

2015 Year 06 Month 02 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

2015 Year 06 Month 02 Day

Date of IRB


Anticipated trial start date

2015 Year 06 Month 02 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 05 Month 02 Day

Last modified on

2016 Year 11 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020000


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name