| 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) |
| 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 |
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| Condition | ||
| Condition | Patients with end-stage renal failure undergoing hemodialysis | |
| Classification by specialty |
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| 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
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| 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 |
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| Age-upper limit |
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| 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 |
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| Key exclusion criteria | 1) Patients in conjunction with blood purification therapies other than HD or OHDF
2) Pregnant or lactating patients |
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| Target sample size | 751 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| 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 | ||||||
| kokada@minos.ocn.ne.jp | |||||||
| Public contact | |||||||
| Name of contact person |
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| 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 | |||||||
| 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 |
| 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 |
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| 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 |
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| Date of IRB |
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| Anticipated trial start date |
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| Last follow-up date |
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| Date of closure to data entry | |||||||
| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Other | |
| Other related information | Observational study |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048924 |