UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000025309
Receipt number R000029112
Scientific Title Effect of acupuncture on cerebral blood flow in healthy adults - Evaluation using arterial spin-labeled magnetic resonance imaging -
Date of disclosure of the study information 2016/12/17
Last modified on 2019/05/16 15:22:16

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Basic information

Public title

Effect of acupuncture on cerebral blood flow in healthy adults - Evaluation using arterial spin-labeled magnetic resonance imaging -

Acronym

Effect of acupuncture on cerebral blood flow in healthy adults - Evaluation using arterial spin-labeled magnetic resonance imaging -

Scientific Title

Effect of acupuncture on cerebral blood flow in healthy adults - Evaluation using arterial spin-labeled magnetic resonance imaging -

Scientific Title:Acronym

Effect of acupuncture on cerebral blood flow in healthy adults - Evaluation using arterial spin-labeled magnetic resonance imaging -

Region

Japan


Condition

Condition

healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Under the concept that acupuncture being one of the traditional Asian medicines fostered over thousands of years contributes to alleviation of many diseases and symptoms not only through mere local reactions but also through the reactions of autonomic nerve system mediated by the high-level central nervous system and immunological/endocrine functions, we have investigated the influences of acupuncture on various body functions and on mainly painful affections.
Then, in this study, using ASLMRI which is safe, noninvasive and repeatable, we will compare changes in cerebral blood flow before and after acupuncture treatment. We examine the influence of acupuncture on the cerebral blood flow of healthy adults and clarify the mechanism by which acupuncture is involved in the high-level central nervous system.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

cerebral blood flow

Key secondary outcomes

Hamilton Depression Rating Scale(HAMD)


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

acupuncture

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

18 years-old <=

Age-upper limit

65 years-old >=

Gender

Male and Female

Key inclusion criteria

healthy adults

Key exclusion criteria

1)Those with experience of causing claustrophobic reaction.
2)Those with wearing a cardiac pacemaker or holding a prosthetic heart valve.
3)Subjects who possesses metals in the body that cannot be confirmed as nonmagnetic (tattoo etc.).
4)Subjects who poor body temperature control.
5)Those who have a history of major depressive disorder or bipolar disorder.
6)Those who have a history of cerebrovascular disorder.

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Tomomi
Middle name
Last name Sakai

Organization

Tokyo Ariake University of Medical and Health Science

Division name

Department of Acupuncture and Moxibustion

Zip code

351-0115

Address

2-9-1 Ariake Koto-ku, Tokyo 135-0063 Japan

TEL

+08-3-6703-7000

Email

sakai@tau.ac.jp


Public contact

Name of contact person

1st name Tomomi
Middle name
Last name Sakai

Organization

Tokyo Ariake University of Medical and Health Science

Division name

Department of Acupuncture and Moxibustion

Zip code

351-0115

Address

2-9-1 Ariake Koto-ku, Tokyo 135-0063 Japan

TEL

+08-3-6703-7000

Homepage URL


Email

sakai@tau.ac.jp


Sponsor or person

Institute

1)Tokyo Ariake University of Medical and Health Science
2)Saitama Medical University

Institute

Department

Personal name



Funding Source

Organization

Tokyo Ariake University of Medical and Health Science

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tokyo Ariake University of Medical and Health Science

Address

2-9-1 Ariake Koto-ku, Tokyo 135-0063 Japan

Tel

+08-3-6703-7000

Email

kida@tau.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

埼玉医科大学総合医療センター(埼玉県)


Other administrative information

Date of disclosure of the study information

2016 Year 12 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

15

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

2016 Year 11 Month 22 Day

Date of IRB

2017 Year 05 Month 11 Day

Anticipated trial start date

2017 Year 06 Month 14 Day

Last follow-up date

2017 Year 09 Month 09 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 12 Month 17 Day

Last modified on

2019 Year 05 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029112


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name