UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000002218
Receipt number R000002725
Scientific Title A randomized trial to assess the effects of hydrogen-ride dissolution water for the patients with mild cognitive impairment (MCI).
Date of disclosure of the study information 2009/07/17
Last modified on 2013/04/01 22:45:46

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Basic information

Public title

A randomized trial to assess the effects of hydrogen-ride dissolution water for the patients with mild cognitive impairment (MCI).

Acronym

An interventional trial for MCI using hydrogen-ride water.

Scientific Title

A randomized trial to assess the effects of hydrogen-ride dissolution water for the patients with mild cognitive impairment (MCI).

Scientific Title:Acronym

An interventional trial for MCI using hydrogen-ride water.

Region

Japan


Condition

Condition

mild cognitive impairment

Classification by specialty

Psychiatry

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine whether hydrogen dissolution water is superior to water (placebo) in prevention of cognitive decline among patients with MCI.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Phase II,III


Assessment

Primary outcomes

Score in Japanese version of ADAS-Cog and Mini Mental State Examination.

Key secondary outcomes

Scores in Japanese version of ADCS-ADL, MRI and SPCET imaging, and Geriatric Depression Scale.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

YES

Dynamic allocation

YES

Institution consideration

Institution is considered as a block.

Blocking

YES

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

The patients of hydrogen group will be intervened with 500ml hydrogen dissolution water every-day for 2 years.

Interventions/Control_2

The patients of placebo group will be intervened with 500ml ordinary water every-day for 2 years.

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

67 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1) Participants of the Tone project.
2) Being able to give a written informed consent to the participation in the present study.
3) Having diagnosis of the mild cognitive impairment.
4) Being able to observe the following requirement: good compliance with the water; participation in the scheduled examinations for assessment; keeping a log-diary recording the consumption of the water.
5) Having a modified Hachinski Ischemic score of 4 or less.
6) Having the 15-item Geriatric Depression Scale score of 6 or less.

Key exclusion criteria

1) Meeting DSM-IV TR criteria for dementing illnesses.
2) Having serious or unstable illnesses.
3) Having a history within past 5 years of serious infectious disease affecting the brain and/or malignant diseases.
4) Having a history of alcohol or drug abuse or dependence (on DSM-IV TR) within the past 5 years.
5) Receiving any types of anti-Alzheimer drugs.
6) Recent (within 4 weeks) initiation of medications that affect the central nervous system.

Target sample size

120


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takashi Asada

Organization

University of Tsukuba

Division name

Department of Neuropsychiatry, Institute of Clinical Medicine

Zip code


Address

1-1-1, Tennodai, Tsukuba City, Ibaraki-prefecture, Japan

TEL

+81(29)853-3178

Email



Public contact

Name of contact person

1st name
Middle name
Last name Takashi Asada

Organization

University of Tsukuba

Division name

Department of Neuropsychiatry, Institute of Clinical Medicine

Zip code


Address

1-1-1, Tennodai, Tsukuba City, Ibaraki-prefecture

TEL


Homepage URL


Email

tasada@md.tsukuba.ac.jp


Sponsor or person

Institute

Department of Neuropsychiatry, Institute of Clinical Medicine University of Tsukuba

Institute

Department

Personal name



Funding Source

Organization

Department of Neuropsychiatry, Institute of Clinical Medicine University of Tsukuba

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

Japan


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

2009 Year 07 Month 17 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

2009 Year 06 Month 01 Day

Date of IRB


Anticipated trial start date

2009 Year 07 Month 01 Day

Last follow-up date

2012 Year 01 Month 01 Day

Date of closure to data entry

2012 Year 08 Month 10 Day

Date trial data considered complete

2012 Year 08 Month 10 Day

Date analysis concluded

2012 Year 10 Month 30 Day


Other

Other related information



Management information

Registered date

2009 Year 07 Month 17 Day

Last modified on

2013 Year 04 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000002725


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name