UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000003390
Receipt number R000004115
Scientific Title Evaluation of effectiveness and safety of hemofilter "Excelflo"(AEF) by continuous hemofiltration treatment for patients who suffer from acute renal failure.
Date of disclosure of the study information 2010/07/01
Last modified on 2012/06/29 10:42:54

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Basic information

Public title

Evaluation of effectiveness and safety of hemofilter "Excelflo"(AEF) by continuous hemofiltration treatment for patients who suffer from acute renal failure.

Acronym

Evaluation of effectiveness of hemofilter "EXCELFLO"

Scientific Title

Evaluation of effectiveness and safety of hemofilter "Excelflo"(AEF) by continuous hemofiltration treatment for patients who suffer from acute renal failure.

Scientific Title:Acronym

Evaluation of effectiveness of hemofilter "EXCELFLO"

Region

Japan


Condition

Condition

SIRS patients who suffer from acute renal failure

Classification by specialty

Emergency medicine Intensive care medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

A comparative study of continuous hemofilter "EXCELFLO" effectiveness of filtration periods, biocompatibility, and the safety of PANFLO-APF by continuous hemodiafiltration treatment (CHDF).

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Amount of adsorbed LDH and fiburin on the membrane after treatment

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

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

EXCELFLO - PANFLO

Interventions/Control_2

PANFLO - EXCELFLO

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

16 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who are 16 years of age and older who suffer from acute renal failure and SIRS.

Key exclusion criteria

1.Patients who are pregnant or maybe pregnant.
2.Children under 15 years of age.
3.Patients who may possibly be at high risk after consulting with a doctor.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takahisa Kawashima

Organization

Kobe University Hospital

Division name

Emergency Critical Care Medicine

Zip code


Address

7-5-2, Kusunoki-cho, Chuo-ku, Kobe-city

TEL

078-382-6521

Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Kobe University Hospital

Division name

Emergency Critical Care Medicine

Zip code


Address


TEL


Homepage URL


Email



Sponsor or person

Institute

Kobe University Hospital
Emergency Critical Care Medicine

Institute

Department

Personal name



Funding Source

Organization

Asahi Kasei Kuraray Medical Co., Ltd.

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


Address


Tel


Email



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

2010 Year 07 Month 01 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

Completed

Date of protocol fixation

2010 Year 04 Month 21 Day

Date of IRB


Anticipated trial start date

2010 Year 09 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2010 Year 03 Month 28 Day

Last modified on

2012 Year 06 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000004115


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name