UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027138
Receipt number R000031092
Scientific Title Study on the effect of blood purification therapy on the immune system
Date of disclosure of the study information 2017/05/01
Last modified on 2019/04/29 14:24:31

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Basic information

Public title

Study on the effect of blood purification therapy on the immune system

Acronym

Study on the effect of blood purification therapy on the immune system

Scientific Title

Study on the effect of blood purification therapy on the immune system

Scientific Title:Acronym

Study on the effect of blood purification therapy on the immune system

Region

Japan


Condition

Condition

All diseases requiring blood purification therapy

Classification by specialty

Nephrology Neurology Clinical immunology
Intensive care medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to investigate the effects on autoimmune diseases, renal failure, septicemia, etc. on the immune system brought about by blood purification therapy and to use it for the treatment and selection of the target disease is there.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Number og Myeroid-derived suppressor cells

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

16 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Cases in which various blood purification therapy is performed in our artificial kidney section and intensive care section.

Key exclusion criteria

Cases in which consent was not obtained.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shigeto Oda

Organization

Chiba University Graduate school of medicine and Chiba University Hospital

Division name

Department of Emergency and Critical Care Medicine an department of Artificial Kidney

Zip code


Address

1-8-1Inohana Chuoku Chiba City and Chiba,Japan

TEL

043-222-7171

Email

nanayayacar@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hanae Wakabayashi

Organization

Chiba University Graduate school of medicine and Chiba University Hospital

Division name

Department of Emergency and Critical Care Medicine an department of Artificial Kidney

Zip code


Address

1-8-1Inohana Chuoku Chiba City and Chiba,Japan

TEL

043-222-7171

Homepage URL


Email

nanayayacar@yahoo.co.jp


Sponsor or person

Institute

Chiba-University Hospital

Institute

Department

Personal name



Funding Source

Organization

Scholarship donation

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

2017 Year 05 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

No longer recruiting

Date of protocol fixation

2016 Year 09 Month 01 Day

Date of IRB

2016 Year 09 Month 01 Day

Anticipated trial start date

2016 Year 12 Month 08 Day

Last follow-up date

2019 Year 03 Month 30 Day

Date of closure to data entry

2019 Year 03 Month 30 Day

Date trial data considered complete

2019 Year 03 Month 30 Day

Date analysis concluded



Other

Other related information

Blood tests before and after treatment, blood tests after remission are performed and data analysis is in progress.


Management information

Registered date

2017 Year 04 Month 26 Day

Last modified on

2019 Year 04 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031092


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name