UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000044708
Receipt number R000051064
Scientific Title Daily change of ultrafiltration volume in patients with combination therapy for peritoneal dialysis and hemodialysis
Date of disclosure of the study information 2023/01/01
Last modified on 2023/07/01 12:19:25

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Basic information

Public title

Daily change of ultrafiltration volume in patients with combination therapy for peritoneal dialysis and hemodialysis

Acronym

Daily change of ultrafiltration volume in PD+HD therapy

Scientific Title

Daily change of ultrafiltration volume in patients with combination therapy for peritoneal dialysis and hemodialysis

Scientific Title:Acronym

Daily change of ultrafiltration volume in PD+HD therapy

Region

Japan


Condition

Condition

patients with combination therapy for peritoneal dialysis and hemodialysis

Classification by specialty

Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the factor for influence daily change of ultrafiltration volume in PD+HD therapy

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

daily change of ultrafiltration volume by peritoneal dialysis

Key secondary outcomes

daily change of ultrafiltration volume by glucose dialysate, daily change of ultrafiltration volume by icodextrin dialysate, patients background, CTR, BNP, blood pressure, D/P Cr, D/D0 Glu, Alb, CRP, Na


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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

patients with combination therapy for peritoneal dialysis and hemodialysis

Key exclusion criteria

none

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Naohiro
Middle name
Last name Toda

Organization

Kansai Electric Power Hospital

Division name

Nephrology

Zip code

553-0003

Address

2-1-7, Fukushima, Fukushima-ku 54

TEL

+81-6-6458-5821

Email

natoda@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name Naohro
Middle name
Last name Toda

Organization

Kansai Electric Power Hospital

Division name

Nephrology

Zip code

553-0003

Address

2-1-7, Fukushima, Fukushima-ku 54

TEL

+81-6-6458-5821

Homepage URL


Email

natoda@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Kansai Electric Power Hospital

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

Ethics community of Kansai Electric Power Hospital

Address

2-1-7, Fukushima, Fukushima-ku 54

Tel

+81-6-6458-5821

Email

natoda@kuhp.kyoto-u.ac.jp


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

2023 Year 01 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

25

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

2020 Year 10 Month 21 Day

Date of IRB

2020 Year 10 Month 21 Day

Anticipated trial start date

2021 Year 01 Month 01 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

none


Management information

Registered date

2021 Year 06 Month 29 Day

Last modified on

2023 Year 07 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000051064


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name