UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000025964
Receipt number R000029849
Scientific Title The relationship between glycemic variability and baroreflex sensitivity in type 2 diabetic patients
Date of disclosure of the study information 2017/02/28
Last modified on 2018/01/06 12:04:14

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Basic information

Public title

The relationship between glycemic variability and baroreflex sensitivity in type 2 diabetic patients

Acronym

Jikei tsuruoka glycemic variability and baroreflex sensitivity study

Scientific Title

The relationship between glycemic variability and baroreflex sensitivity in type 2 diabetic patients

Scientific Title:Acronym

Jikei tsuruoka glycemic variability and baroreflex sensitivity study

Region

Japan


Condition

Condition

Type 2 diabetes

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To verify the relationship between glycemic variability and baroreflex sensitivity in type 2 diabetic patients.

Basic objectives2

Others

Basic objectives -Others

To verify relationship between intima media thickness of the carotid artery and baroreflex sensitivity in type 2 diabetic patients.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Coefficient of variation for glycemic variability and baroreflex sensitivity

Key secondary outcomes

・Standard deviation for glycemic variability and baroreflex sensitivity
・Mean amplitude of glycemic excursions for glycemic variability and baroreflex sensitivity
・Fasting plasma glucose and baroreflex sensitivity
・HbA1c and baroreflex sensitivity
・Intima media thickness of the carotid artery and baroreflex sensitivity
・Flow mediated dilation and baroreflex sensitivity


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

・Hospitalized type 2 diabetic patients

Key exclusion criteria

・having arrhythmia
・receiving non-dihydropyridine calcium channel blockers
・receiving digitalis
・receiving antipsychotics
・having severe renal dysfunction (serum Cr > 2.5 mg/dl)
・having severe liver dysfunction (3 X the upper limit of normal)
・having severe infection, severe trauma, or pre and post operation
・having diabetic ketosis, diabetic coma, or insulin-dependent diabetes mellitus
・being pregnant
・having malignancy
・being unsuitable for participation in the trial for any reason, according to the investigators
・having myocardial infarction, heart failure or cerebral infarction within a half year
・heavy drinker

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Daisuke Matsutani

Organization

The Jikei University School of Medicine

Division name

Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine

Zip code


Address

3-25-8 Nishi-Shinbashi, Minato-ku, Tokyo

TEL

03-3433-1111

Email

daisuke19870116@jikei.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Daisuke Matsutani

Organization

The Jikei University School of Medicine

Division name

Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine

Zip code


Address

3-25-8 Nishi-Shinbashi, Minato-ku, Tokyo

TEL

03-3433-1111

Homepage URL


Email

daisuke19870116@jikei.ac.jp


Sponsor or person

Institute

The Jikei University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Selt funding

Organization

Division

Category of Funding Organization

Self funding

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

2017 Year 02 Month 28 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

2017 Year 02 Month 28 Day

Date of IRB


Anticipated trial start date

2017 Year 02 Month 28 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The prospective study


Management information

Registered date

2017 Year 02 Month 01 Day

Last modified on

2018 Year 01 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029849


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name