UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000057577 |
|---|---|
| Receipt number | R000065284 |
| Scientific Title | A retrospective clinical study of mortality according to hemoglobin levels and administration of calcimimetics and erythropoietin stimulating agents in patients on hemodialysis using dialyzers with beta2-microglobulin clearance of more than 70 mL/min and on online hemodialfiltration. |
| Date of disclosure of the study information | 2026/03/31 |
| Last modified on | 2025/10/10 14:16:32 |
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Basic information
Public title
A retrospective clinical study of mortality according to hemoglobin levels and administration of calcimimetics and erythropoietin stimulating agents in dialysis patients.
Acronym
Influence of mortality according to hemoglobin levels and administration of calcimimetics and erythropoietin stimulating agents in dialysis patients.
Scientific Title
A retrospective clinical study of mortality according to hemoglobin levels and administration of calcimimetics and erythropoietin stimulating agents in patients on hemodialysis using dialyzers with beta2-microglobulin clearance of more than 70 mL/min and on online hemodialfiltration.
Scientific Title:Acronym
Influence of mortality according to hemoglobin levels and administration of calcimimetics and erythropoietin stimulating agents in HD using dialyzers with beta2-microglobulin clearance of more than 70 mL/min 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
A propensity score matching model and adjusted Cox regression analysis is used in a retrospective 2-year observational study. The effects of mortality in patients within target Hb range grouping by users and non-users with ESAs and/or calcimimetics . In addition, chi-square tests is performed to assess the 1-year and 2-year mortality on patients whose Hb values are within and outside the target range grouping by users and non-users with ESAs and/or calcimimetics.
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 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 hemodialysis and online hemodiafiltration
5 Dialysis frequency below 3 sessions per week or dialysis time below 3 hour per session
6 pre-OHDF substitution volume of <60 L and post-OHDF substitution volume of <8 L
7 Cases <20 years old
8 For propensity score matching, Hb <10g/dL and >12.9g/dL
Target sample size
738
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
7700011
Address
6-1 Kitasako ichiban-cho, Tokushima-shi, Tokushima, Japan
TEL
0886310110
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
7700011
Address
6-1 Kitasako ichiban-cho, Tokushima-shi, Tokushima, Japan
TEL
08081571675
Homepage URL
m.tashiro@khg.or.jp
Sponsor or person
Institute
Social medical corporation Kawashimakai Kawashima Hospital
Institute
Department
Personal name
Funding Source
Organization
Nothing
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
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
783
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
Terminated
Date of protocol fixation
| 2025 | Year | 03 | Month | 08 | Day |
Date of IRB
| 2025 | Year | 04 | Month | 08 | Day |
Anticipated trial start date
| 2025 | Year | 04 | Month | 15 | Day |
Last follow-up date
| 2025 | Year | 08 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
In this retrospective 2-year observational study, we compare the 2-year mortality in patients within target Hb range grouping by users and non-users with ESAs and/or calcimimetics. 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 or cases outside the target Hb range were annually censored by checking the use of ESAs, HIF-PH inhibitors, calcimimetics, and dialysis method (HD, pre-dilution OHDF, and post-dilution OHDF). We then performed Cox proportional hazards analysis with adjustments. In addition, we perform chi-square tests to evaluate the 1-year and 2-year mortality in patients within and outside the target Hb range grouping by users and non-users with ESAs and/or calcimimetics. The 1-year mortality and 2-year mortality are expressed as the ratio of 1-year and 2-year deaths to the number of patients in each group.
Management information
Registered date
| 2025 | Year | 04 | Month | 10 | Day |
Last modified on
| 2025 | Year | 10 | Month | 10 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065284
