UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027271
Receipt number R000031243
Scientific Title Observational study on postoperative cognitive function of the patients with cardiovascular surgery and the intestinal flora
Date of disclosure of the study information 2017/10/01
Last modified on 2017/05/08 16:25:39

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Basic information

Public title

Observational study on postoperative cognitive function of the patients with cardiovascular surgery and the intestinal flora

Acronym

Observational study on postoperative cognitive function of the patients with cardiovascular surgery and the intestinal flora

Scientific Title

Observational study on postoperative cognitive function of the patients with cardiovascular surgery and the intestinal flora

Scientific Title:Acronym

Observational study on postoperative cognitive function of the patients with cardiovascular surgery and the intestinal flora

Region

Japan


Condition

Condition

Conditions requiring cardiac or great vessel surgery

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to investigate the relation between the effect on post operative cognitive function of cardiac and great vessel surgery using cardio-pulmonary bypass and the intestinal bacteria

Basic objectives2

Bio-availability

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Correlation between distribution change of intestinal flora before and after cardiac surgery using cardio-pulmonary bypass and postoperative cognitive function

Key secondary outcomes

Correlation between intestinal flora distribution and various examination results, postoperative renal function and cardiac function


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

15 years-old <=

Age-upper limit

85 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Patients who agreed to participate in the main research "Intestinal Flora - Cardiac Surgery STUDY"
2) Patients who got consent to participate in collateral research by written document

Key exclusion criteria

1) Patients who are judged by the investigator or shared medical doctor to be unsuitable for participation in the accompanying examination

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yosuke Kubota

Organization

National Cerebral and Cardiovascular Center

Division name

Department of Anesthesiology

Zip code


Address

Suitashi Fujishirodai 5chome 7bann 1

TEL

08052497049

Email

carvy26@me.com


Public contact

Name of contact person

1st name
Middle name
Last name Kenji Yoshitani

Organization

National Cerebral and Cardiovascular Center

Division name

Department of Anesthesiology

Zip code


Address

Suitashi Fujishirodai 5chome 7bann 1

TEL

0668335012

Homepage URL


Email

sohtamikaze@gmail.com


Sponsor or person

Institute

Department of Anesthesiology

Institute

Department

Personal name



Funding Source

Organization

Cardiovascular R & D expenses

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

2017 Year 10 Month 01 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

Preinitiation

Date of protocol fixation

2017 Year 10 Month 01 Day

Date of IRB


Anticipated trial start date

2017 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

nothing


Management information

Registered date

2017 Year 05 Month 08 Day

Last modified on

2017 Year 05 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031243


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name