UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000034829
Receipt number R000039723
Scientific Title Effects of burdock sprout extract on decreasing blood glucose level; A single center double blind randomized controlled trial
Date of disclosure of the study information 2018/12/01
Last modified on 2021/09/27 14:48:03

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Basic information

Public title

Effects of burdock sprout extract on decreasing blood glucose level; A single center double blind randomized controlled trial

Acronym

Study for effects of burdock sprout extract on decreasing blood glucose level

Scientific Title

Effects of burdock sprout extract on decreasing blood glucose level; A single center double blind randomized controlled trial

Scientific Title:Acronym

Study for effects of burdock sprout extract on decreasing blood glucose level

Region

Japan


Condition

Condition

impaired glucose tolerance, diabetes mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate effects of burdock sprout extract on decreasing blood glucose level and other factors such as HbA1c in the patients whose blood glucose level is higher than normal range even after nutritional guidance or taking dipeptidyl peptidase-4 (DPP4) inhibitor.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Decrease in blood glucose level or HbA1c in the patients whose blood glucose level is higher than normal range at 4 and 12 weeks after taking burdock sprout extract.

Key secondary outcomes

Change of body weight, liver function, serum lipid levels, insulin level, GLP-1, HOMA-IR, ghrelin level and adipokine levels such as leptin and adiponectine in the patients whose blood glucose level is higher than normal range at 4 and 12 weeks after taking burdock sprout extract.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

burdock sprout extract (+)

Interventions/Control_2

burdock sprout extract (-)

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

65 years-old >

Gender

Male and Female

Key inclusion criteria

1. A patient whose fasting blood glucose level is over 110 mg/dL, or casual blood glucose level is over 125 mg/dL, or HbA1c is over 6.5%
2. A patient who attended nutritional guidance 4 weeks or more before starting this study

Key exclusion criteria

1. A patient who is taking any drugs for diabetes mellitus other than DPP4 inhibitor
2. A patient who cannot stop any supplements health food affecting blood glucose level
3. A patient who is pregnant, or may become pregnant, or desire to get pregnant
4. A patient who has or had serious diseases in heart, liver, kidney, gastrointestinal tract, etc.
5. A patient who has allergy for any drugs or food
6. A patient who has or had drug or alcohol dependence
7. A patient who is judged to be unsuitable for this study by the doctor

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Yoshinori
Middle name
Last name Horie

Organization

Shonan Keiiku Hospital

Division name

Internal Medicine

Zip code

252-0816

Address

4360 Endo Fujisawa-shi Kanagawa-ken, 252-0816, Japan

TEL

0466-48-0050

Email

y-horie@keiiku.gr.jp


Public contact

Name of contact person

1st name Kenji
Middle name
Last name Miyazaki

Organization

Shonan Keiiku Hospital

Division name

Office

Zip code

252-0816

Address

4360 Endo Fujisawa-shi Kanagawa-ken, 252-0816, Japan

TEL

0466-48-0050

Homepage URL


Email

k-miyazaki@keiiku.gr.jp


Sponsor or person

Institute

Shonan Keiiku Hospital

Institute

Department

Personal name



Funding Source

Organization

Kracie Holdings Co. Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

Keio University, Graduate School of Media and Governance

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Shonan Keiiku Hospital

Address

4360 Endo Fujisawa-shi Kanagawa-ken, 252-0816, Japan

Tel

0466-48-0050

Email

k-miyazaki@keiiku.gr.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



Other administrative information

Date of disclosure of the study information

2018 Year 12 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

Terminated

Date of protocol fixation

2018 Year 11 Month 08 Day

Date of IRB

2018 Year 07 Month 23 Day

Anticipated trial start date

2018 Year 12 Month 01 Day

Last follow-up date

2019 Year 12 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 11 Month 09 Day

Last modified on

2021 Year 09 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000039723


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name