UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057263
Receipt number R000063951
Scientific Title Effect of Different Hemofilters Used in Continuous Renal Replacement Therapy on the Prognosis of Septic Acute Kidney Injury
Date of disclosure of the study information 2025/03/12
Last modified on 2025/09/12 11:19:44

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Basic information

Public title

Effect of Different Hemofilters Used in Continuous Renal Replacement Therapy on the Prognosis of Septic Acute Kidney Injury

Acronym

Effect of Different Hemofilters Used in Continuous Renal Replacement Therapy on the Prognosis of Septic Acute Kidney Injury

Scientific Title

Effect of Different Hemofilters Used in Continuous Renal Replacement Therapy on the Prognosis of Septic Acute Kidney Injury

Scientific Title:Acronym

Effect of Different Hemofilters Used in Continuous Renal Replacement Therapy on the Prognosis of Septic Acute Kidney Injury

Region

Japan


Condition

Condition

sepsis

Classification by specialty

Intensive care medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Comparative Study of Cytokine Adsorption Clearance and Mortality Rates with Hemofilters Used in Continuous Renal Replacement Therapy in the ICU

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Phase I


Assessment

Primary outcomes

Cytokine Adsorption Clearance

Key secondary outcomes

1.28days survival rate
2.Changes in Various Measured Parameters Before and After the Hemofilter
3.Correlation Between Changes in Measured Parameters and Severity Scores
4.Trend of SOFA Scores Over 7 Days from the Start of CKRT
5.Trend of Catecholamine Index Over 7 Days from the Start of CKRT
6.Trend of P/F Ratio Over 7 Days from the Start of CKRT


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Blood purification using AN69ST hemofilter

Interventions/Control_2

Blood purification using PS hemofilter

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.>=20 years of old
2.sepsis
3.Patients for whom the attending physician determined that continuous renal replacement therapy (CRRT) was necessary

Key exclusion criteria

1.Patients from whom consent was not obtained
2.Patients post-cardiopulmonary resuscitation
3.Pregnant patients
4.Individuals deemed unsuitable for participation in the study by the researchers

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Yoshihiko
Middle name
Last name Nakamura

Organization

Faculty of Medicine,Fukuoka University

Division name

Department of Emergency and Critical Care Medicine

Zip code

8140180

Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan

TEL

092-801-1011

Email

nakamura58@fukuoka-u.ac.jp


Public contact

Name of contact person

1st name Yoshihiko
Middle name
Last name Nakamura

Organization

Faculty of Medicine,Fukuoka University

Division name

Department of Emergency and Critical Care Medicine

Zip code

8140180

Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan

TEL

092-801-1011

Homepage URL


Email

pdmxy827@yahoo.co.jp


Sponsor or person

Institute

Fukuoka University

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Fukuoka University Hospital Clinical Resarch Assist Center

Address

7-45-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan

Tel

092-801-1011

Email

rinshou@adm.fukuoka-u.ac.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

福岡大学病院 救命救急センター


Other administrative information

Date of disclosure of the study information

2025 Year 03 Month 12 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

Open public recruiting

Date of protocol fixation

2025 Year 03 Month 10 Day

Date of IRB

2025 Year 03 Month 10 Day

Anticipated trial start date

2025 Year 04 Month 01 Day

Last follow-up date

2030 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 03 Month 12 Day

Last modified on

2025 Year 09 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063951