UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051791
Receipt number R000059102
Scientific Title Retrospective clinical study for comparison between membrane materials on survival in super high flux hemodialysis and online hemodiafiltration
Date of disclosure of the study information 2024/03/31
Last modified on 2023/08/02 12:06:54

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Basic information

Public title

Study for comparison between membrane materials on survival in super high flux hemodialysis and online hemodiafiltration

Acronym

Prognosis study of membrane materials in SHF-HD and OHDF

Scientific Title

Retrospective clinical study for comparison between membrane materials on survival in super high flux hemodialysis and online hemodiafiltration

Scientific Title:Acronym

Prognosis verification of membrane materials in SHF-HD and OHDF

Region

Japan


Condition

Condition

Patients with end-stage kidney disease undergoing super high flux hemodialysis and online hemodiafiltration

Classification by specialty

Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We compare 3-year all-cause mortality between polyethersufone membrane and other membranes in super high flux hemodialysis and online hemodiafiltration with beta2-microglobulin clearance of more than 70 mL/min

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

3-year all-cause mortality

Key secondary outcomes

Estimated albumin leakage


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 and online hemodiafiltration as of July 1, 2017

Key exclusion criteria

1. Under 20 years of age
2. Dialysis conditions between April 1, 2017 and June 30, 2017, which are different from those as of July 1, 2017
3. Blood purification methods other than hemodialysis and online hemodiafiltration
4. Dialysis frequency below 3 sessions/week or dialysis time below 3 hours/session
5. Pregnant or lactating patients
6. Missing data for covariates at study entry
7. Dialyzers with beta2 microgloburln clearance below 70 mL/min
8. Dialyzers and hemodiafilters less than 50 number of each membrane material

Target sample size

700


Research contact person

Name of lead principal investigator

1st name Kazuyoshi
Middle name
Last name Okada

Organization

Social medical corporation Kawashimakai Kawashima Hospital

Division name

Blood purification management center

Zip code

770-0011

Address

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

TEL

81-88-631-0110

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

81-88-631-0110

Homepage URL


Email

m.tashiro@khg.or.jp


Sponsor or person

Institute

Social medical corporation, Kawashimakai, Kawashima hospital

Institute

Department

Personal name



Funding Source

Organization

Social medical corporation, Kawashimakai, 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

Social medical corporation, Kawashimakai, Kawashima hospital, Research Ethics Review Committee

Address

6-1 Kitasakoichiban-cho, Tokushima-shi

Tel

+81886310110

Email

nekooken@khg.or.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

2024 Year 03 Month 31 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

2023 Year 07 Month 18 Day

Date of IRB

2023 Year 08 Month 01 Day

Anticipated trial start date

2023 Year 08 Month 03 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Observational study


Management information

Registered date

2023 Year 08 Month 02 Day

Last modified on

2023 Year 08 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000059102


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name