UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027835
Receipt number R000031871
Scientific Title Comparison of weight loss effect of diabetes treatment for obese type 2 diabetic patients.
Date of disclosure of the study information 2017/06/26
Last modified on 2017/06/20 09:01:07

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Basic information

Public title

Comparison of weight loss effect of diabetes treatment for obese type 2 diabetic patients.

Acronym

Comparison of weight loss effect of diabetes treatment for obese type 2 diabetic patients.

Scientific Title

Comparison of weight loss effect of diabetes treatment for obese type 2 diabetic patients.

Scientific Title:Acronym

Comparison of weight loss effect of diabetes treatment for obese type 2 diabetic patients.

Region

Japan


Condition

Condition

Diabetes

Classification by specialty

Medicine in general

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

By bariatric surgery on obese type 2 diabetic patients, not only weight loss effect but also metabolic improvement effect can be expected. However, bariatric surgery, which is applied for insurance in Japan, is only sleeve gastrectomy. Patients with obesity, which is an indication for surgery, are, in principle, patients with primary obesity between the ages of 18 and 65, and there is no significant weight loss and no improvement in obesity related complications despite medical treatments for more than 6 months.
Until recently, although diabetes treatment have an effect of improving blood glucose, body weight gain accompanying treatment became a problem.
GLP-1 receptor agonist and SGLT2 inhibitor are on the market. I evaluated the effect of GLP-1 receptor agonist and SGLT-2 inhibitor on obese type 2 diabetic patients on the parameters of blood glucose and BMI.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

HbA1c(0M,6M)

Key secondary outcomes

BMI(0M,6M)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

The group treated with GLP-1 receptor agonist(Duration:6 months)

Interventions/Control_2

The group treated with SGLT-2 inhibitor(Duration:6 months)

Interventions/Control_3

The group treated with GLP-1 receptor agonist and SGLT-2 inhibitor(Duration:6 months)

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

BMI>=22.0

Key exclusion criteria

Renal dysfunction(eGFR>=30mL/min/1.73m2)

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takahisa Hasegawa

Organization

KYORITSU HOSPITAL

Division name

internal medicine

Zip code


Address

16-5, Chuo-cho, Kawanishi-city,Hyogo

TEL

072-758-1131

Email

h.taka517@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Takahisa Hasegawa

Organization

KYORITSU HOSPITAL

Division name

internal medicine

Zip code


Address

16-5, Chuo-cho, Kawanishi-city,Hyogo

TEL

072-758-1131

Homepage URL


Email

h.taka517@gmail.com


Sponsor or person

Institute

KYORITSU HOSPITAL

Institute

Department

Personal name



Funding Source

Organization

KYORITSU HOSPITAL

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

協立病院


Other administrative information

Date of disclosure of the study information

2017 Year 06 Month 26 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

2015 Year 03 Month 01 Day

Date of IRB


Anticipated trial start date

2015 Year 04 Month 01 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

2017 Year 06 Month 20 Day

Last modified on

2017 Year 06 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031871


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name