UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000042935
Receipt No. R000048924
Scientific Title Retrospective clinical study for prognosis verification of online hemodiafiltration
Date of disclosure of the study information 2021/01/15
Last modified on 2021/07/22 (Ver. 3)

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Basic information
Public title Retrospective clinical study for prognosis verification of online hemodiafiltration
Acronym Prognosis verification of O-HDF
Scientific Title Retrospective clinical study for prognosis verification of online hemodiafiltration
Scientific Title:Acronym Prognosis verification of O-HDF
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 the prognosis of O-HDF and the factors influencing the prognosis
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes 1-to-3 years prognosis and event incidence rate
Key secondary outcomes The factors influencing the prognosis

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 1) The age is 20 years or older, regardless of gender, hospitalization / outpatient, medical history, complications, or medical history.
2) Cases in which dialysis treatment from April 1, 2017 to June 30, 2017 is the same as dialysis treatment as of July 1, 2017
3) Cases with dialysis time of 3 hours or more/session and dialysis frequency of 3 sessions/week
Key exclusion criteria 1) Patients in conjunction with blood purification therapies other than HD or OHDF
2) Pregnant or lactating patients
Target sample size 751

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 1-39 Kitasako ichiban-cho, Tokushima city, Tokushima,Japan
TEL 088-631-0110
Email kokada@minos.ocn.ne.jp

Public contact
Name of contact person
1st name Hiroyuki
Middle name
Last name Michiwaki
Organization Social medical corporation, Kawashimakai, Kawashima hospital
Division name Department of Clinical Engineering
Zip code 770-0011
Address 1-39 Kitasako ichiban-cho, Tokushima city, Tokushima,Japan
TEL 088-631-0110
Homepage URL
Email michiwaki@khg.or.jp

Sponsor
Institute Social medical corporation Kawashimakai
Institute
Department

Funding Source
Organization Nipro Corporation
Organization
Division
Category of Funding Organization Profit organization
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
Address 1-39 Kitasako ichiban-cho, Tokushima city, 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
2021 Year 01 Month 15 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 751
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
2020 Year 12 Month 22 Day
Date of IRB
2021 Year 01 Month 05 Day
Anticipated trial start date
2021 Year 02 Month 01 Day
Last follow-up date
2021 Year 06 Month 30 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
2021 Year 01 Month 07 Day
Last modified on
2021 Year 07 Month 22 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048924