UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017812
Receipt number R000020636
Scientific Title Evaluation Study of Nutrition Status in the hemodialysis patients with the vitamin E-bonded dialyzer.
Date of disclosure of the study information 2015/06/06
Last modified on 2015/06/04 16:25:11

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Basic information

Public title

Evaluation Study of Nutrition Status in the hemodialysis patients with the vitamin E-bonded dialyzer.

Acronym

Evaluation Study of Nutrition Status in the hemodialysis patients with the vitamin E-bonded dialyzer.

Scientific Title

Evaluation Study of Nutrition Status in the hemodialysis patients with the vitamin E-bonded dialyzer.

Scientific Title:Acronym

Evaluation Study of Nutrition Status in the hemodialysis patients with the vitamin E-bonded dialyzer.

Region

Japan


Condition

Condition

CKD/ESRD

Classification by specialty

Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Hemodialysis patients are at risk of protein-energy malnutrition (PEM).
Oxidative stress and chronic inflammation are the cause of the PEM. The vitamin E-bonded dialyzer (VEM) has anti-inflammatory and anti-nociceptive effects. The aim of this study is to investigate the utility of the VEM for The PEM of hemodialysis patients.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

transthyretin

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

vitamin E-bonded polysulfone membrane dialyzer

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

65 years-old <=

Age-upper limit

90 years-old >

Gender

Male and Female

Key inclusion criteria

Adult human undergoing chronic dialysis therapy.
And the mean of their serum albumin for the three months before this study is less than 3.8g/dl.

Key exclusion criteria

AST or ALT for the three months before this study is more than 20 IU/L.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Nozomu Yamanaka

Organization

National Defense Medical College

Division name

Department of Surgery2

Zip code


Address

Namiki 3-2, Tokorozawa, Saitama 359-8513, Japan

TEL

04-2995-1650

Email

non0101@hotmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Nozomu Yamanaka

Organization

National Defense Medical College

Division name

Department of Surgery2

Zip code


Address

Namiki 3-2, Tokorozawa, Saitama 359-8513, Japan

TEL

04-2995-1650

Homepage URL


Email

non0101@hotmail.com


Sponsor or person

Institute

National Defense Medical College

Institute

Department

Personal name



Funding Source

Organization

Vitamembrane study group

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


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

イムス富士見総合病院(埼玉県)
イムス三芳総合病院(埼玉県)


Other administrative information

Date of disclosure of the study information

2015 Year 06 Month 06 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

Enrolling by invitation

Date of protocol fixation

2014 Year 12 Month 19 Day

Date of IRB


Anticipated trial start date

2015 Year 06 Month 08 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

2015 Year 06 Month 04 Day

Last modified on

2015 Year 06 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020636


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name