UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000059330
Receipt number R000067867
Scientific Title A retrospective clinical study for the contribution of protein-energy wasting, inflammation, and aging in the impact of calcimimetics on survival in patients on hemodialysis and online hemodiafiltration.
Date of disclosure of the study information 2026/03/31
Last modified on 2025/10/08 11:21:35

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Basic information

Public title

A retrospective clinical study for the contribution of protein-energy wasting, inflammation, and aging in the impact of calcimimetics on survival in dialysis patients.

Acronym

The effects of protein-energy wasting, inflammation, and aging on the prognosis of calcimimetics in dialysis patients.

Scientific Title

A retrospective clinical study for the contribution of protein-energy wasting, inflammation, and aging in the impact of calcimimetics on survival in patients on hemodialysis and online hemodiafiltration.

Scientific Title:Acronym

The effects of protein-energy wasting, inflammation, and aging on the prognosis of calcimimetics in patients on HD and OHDF.

Region

Japan


Condition

Condition

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

Classification by specialty

Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We clarify the involvement of protein-energy wasting, inflammation, and aging on 2-year all-cause mortality by calcimimetics in patients on hemodialysis and online hemodiafiltration with in vitro beta2-microglobulin clearance of 70 mL/min and more.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

2-year all-cause mortality

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 hemodialysis as of July 1, 2017

Key exclusion criteria

1 Use of dialyzers with beta2-microgloburln clearance below 70 mL/min
2 Missing data for covariates at study entry
3 Dialysis conditionssuch as dialysis method, dilution method, and membrane material between April 1, 2017 and June 30, 2017, which are different from those as of July 1, 2017
4 Blood purification methods other than HD
5 Dialysis frequency below 3 sessions per week or dialysis time below 3 hour per session
6 Predilution online hemodiafiltration substitution volume of <60 L and postdilution online hemodiafiltration substitution volume of <8 L

Target sample size

783


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

0886310110

Email

kokada@ckdjapan.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

0886310110

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 Committee

Address

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

Tel

088-631-0110

Email

m.tashiro@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

2026 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

2025 Year 09 Month 03 Day

Date of IRB


Anticipated trial start date

2025 Year 10 Month 10 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

In this retrospective observational study, we compare the 2-year mortality on users and non-users of calcimimetics in patients withour protein-energy wasying and inflammation, and patients with protein-energy wasting and/or inflammation. Using a propensity score matching model and Kaplan-Meier method, we daily censored deaths and transfers to other hospitals. In addition, transfers to other group is annually censored by checking the use of calcimimetics, dialysis method (HD, predilution OHDF, and postdilution OHDF), albumin leakage (below 3 g/session and over 3 g/session), and protein-enegy wasting and/or inflammation. We then performed Cox proportional hazards analysis with adjustments for some covariates that remained significantly different between the groups. In addition, we perform the stratified analysis by median age to compare 2-year mortality rate between calcimimetic users and non-users in patients without protein-energy wasting and inflammation, and patients with protein-energy wasting and/or inflammation. Furthermore, we compare cumulative 2-year survival by the Kaplan-Meier method among groups.


Management information

Registered date

2025 Year 10 Month 08 Day

Last modified on

2025 Year 10 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067867