UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019741
Receipt number R000022734
Scientific Title Clinical effects of a peritoneal dialysis fluid with neutral PH , using Automated peritoneal dialysis patients
Date of disclosure of the study information 2015/11/11
Last modified on 2015/11/10 21:30:30

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Clinical effects of a peritoneal dialysis fluid with neutral PH , using Automated peritoneal dialysis patients

Acronym

APD with NeutoralPH fluid study

Scientific Title

Clinical effects of a peritoneal dialysis fluid with neutral PH , using Automated peritoneal dialysis patients

Scientific Title:Acronym

APD with NeutoralPH fluid study

Region

Japan


Condition

Condition

end stage renal disease patients on peritoneal dialysis therapy

Classification by specialty

Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to investigage the influence of dialysis solution with neutral PH fluid in patients on automated peritoneal dialyhsis therapy,by checking inflamatory marker, oxdative stress mareker and clinical conditions.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Others

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

After resistration and 6months after changing dialysate with neutral PH ,inflamatory marker,HsCRP,IL-6,TNF-alfaPrealbumin, Histidine.

Key secondary outcomes

Advanced glycation endproducts both blood and fluid, peritoneal function test, apetite, neutoritional status.


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Change dialysate from asid based fluid to neutral PH fluid using Automated peritoneal dialysis machine for 6months.

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

18 years-old <

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1.under going peritoneal dialysis patients
more than 3 month
2.get informed consent
3.over18 years old. both femal and male

Key exclusion criteria

1.kidney transplantation.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Mari Ishida

Organization

Tokai university Hachioji Hospital

Division name

Nephrology,aEndcrinology and Metabolism

Zip code


Address

1383 ishikawa machi,Hachioji city,Tokyo,Japan

TEL

+81-42-639-1144

Email

marira101213@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Mari Ishida

Organization

Tokai University Hachioji Hospital

Division name

Nephrology

Zip code


Address

1383 ishikawa machi,Hachioji city,Tokyo,Japan

TEL

+81-42-639-1144

Homepage URL


Email

marira101213@gmail.com


Sponsor or person

Institute

Tokai University Hachioji Hospital

Institute

Department

Personal name



Funding Source

Organization

Tokai University Hachioji Hospital

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

BAXTER Limited, Japan

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

北彩都病院 北海道 旭川市


Other administrative information

Date of disclosure of the study information

2015 Year 11 Month 11 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

2010 Year 10 Month 01 Day

Date of IRB


Anticipated trial start date

2010 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



Management information

Registered date

2015 Year 11 Month 10 Day

Last modified on

2015 Year 11 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022734


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name