UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000047948
Receipt number R000054664
Scientific Title Retrospective clinical study to compare survival between super high-flux hemodialysis with high albumin leakage and online hemodiafiltration with low albumin leakage
Date of disclosure of the study information 2022/10/01
Last modified on 2022/12/04 13:58:31

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Basic information

Public title

Retrospective clinical study for albumin leakage and survival between hemodialysis and online hemodiafiltration

Acronym

Prognosis verification albumin leakage between super high-flux HD and OHDF

Scientific Title

Retrospective clinical study to compare survival between super high-flux hemodialysis with high albumin leakage and online hemodiafiltration with low albumin leakage

Scientific Title:Acronym

Prognosis verification of super high-flux hemodialysis with high albumin leakage and online hemodiafiltration with low albumin leakage

Region

Japan


Condition

Condition

Patients with end-stage renal failure undergoing hemodialysis

Classification by specialty

Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We clarify 3-year all-cause mortality in super high-flux HD with high albumin lealage and OHDF with low albumin leakage

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

3-year all-cause mortality during 3 yearss between super high-flux HD with high albumin leakage and OHDF with low albumin leakage

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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients on maintenance hemodialysis or online hemodiafiltration 3 times a week as of July 1, 2017

Key exclusion criteria

1 Under 20 years of age 2 Dialysis conditions including dialysis method, dilution method, substitution volume, membrane material between April 1, 2017 and June 30, 2017, which are different from those as of July 1, 2017 3 Blood purification methods other than HD or OHDF 4 Dialysis frequency below 3 sessions per week or dialysis time below 3 hour per session 5 Substitution volume of less than 60 L in predilution OHDF and less than 8 L in postdilution OHDF 6 Pregnant or lactating patients 7 Missing values of variables at the start of the study 8 Beta2 microglobulin clearance less than 70 mL per min

Target sample size

800


Research contact person

Name of lead principal investigator

1st name Kazuyoshi
Middle name
Last name Okada

Organization

Social medical corporation Kawashimakai

Division name

Blood purification management center

Zip code

770-0011

Address

6-1 Kitasako ichiban-cho, Tokushima-shi, Tokushima,Japan

TEL

088-631-0110

Email

kokada@minos.ocn.ne.jp


Public contact

Name of contact person

1st name Manabu
Middle name
Last name Tashiro

Organization

Social medical corporation, Kawashimakai, Kawashima hospital

Division name

Department of Nephrology

Zip code

770-0011

Address

6-1 Kitasako ichiban-cho, Tokushima-shi, Tokushima,Japan

TEL

088-631-0110

Homepage URL


Email

m.tashiro@khg.or.jp


Sponsor or person

Institute

Kawashima hospital

Institute

Department

Personal name



Funding Source

Organization

Kawashima Hospital

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

Kawashima Hospital

Address

6-1 Kitasako ichiban-cho, Tokushima-shi, Tokushima,Japan

Tel

088-631-0110

Email

kokada@minos.ocn.ne.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

2022 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

Completed

Date of protocol fixation

2022 Year 02 Month 15 Day

Date of IRB

2022 Year 04 Month 12 Day

Anticipated trial start date

2022 Year 07 Month 06 Day

Last follow-up date

2022 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

nothing


Management information

Registered date

2022 Year 06 Month 04 Day

Last modified on

2022 Year 12 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000054664


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name