UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015952
Receipt number R000018559
Scientific Title Study of the change of dietary intake and contents after taking selective SGLT2 inhibitor, Ipragliflozin
Date of disclosure of the study information 2014/12/15
Last modified on 2014/12/15 15:44:34

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Basic information

Public title

Study of the change of dietary intake and contents after taking selective SGLT2 inhibitor, Ipragliflozin

Acronym

Selective SGLT2 inhibitor, Ipragliflozin and the change of a meal

Scientific Title

Study of the change of dietary intake and contents after taking selective SGLT2 inhibitor, Ipragliflozin

Scientific Title:Acronym

Selective SGLT2 inhibitor, Ipragliflozin and the change of a meal

Region

Japan


Condition

Condition

Type 2 diabetes mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

New oral hypoglycemic agent, Ipragliflozin is selective inhibitor of SGLT2 and show the improvement of blood glucose control and the effect of losing weight. We study the efficacy and safety for Ipragliflozin in patients with type 2 diabetes.

Basic objectives2

Others

Basic objectives -Others

Many studies report that the effect of losing weight stops within a certain period. We investigate the change of dietary habit on the hypothesis that a stop of losing weight caused by the change of dietary intake and contents after taking SGLT2 inhibitor, Ipragliflozin.

Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase IV


Assessment

Primary outcomes

We investigate HbA1c, GA, body weight, waist circumstance, body composition, and appearance of harmful phenomenon at initial and screening visits (3 month, 6 month, and 12 month after taking Ipragliflozin).

Key secondary outcomes

We investigate the dietary intake and contents at initial and screening visits (3 month, 6 month, and 12 month after taking Ipragliflozin).


Base

Study type


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

Medicine

Interventions/Control_1

Ipragliflozin

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

1) Patients with type 2 diabetes mellitus
2) Patients with not enough blood glucose control (HbA1c > 7.0%) even if putting dietary therapy, exercise, education for improvement of a daily habit, and medicinal treatment into practice

Key exclusion criteria

1) Patients with allergy for Ipragliflozin
2) Patients got severe ketosis, diabetic coma, and diabetic precoma during the past 6 months
3) Patients with severe infectious disease and injury, and in perioperative
4) Patients with renal dysfunction at a moderate level or high
5) Patients whose doctor judges to unfit for this study

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Murakami Hiroshi

Organization

Hirosaki University Graduate School of Medicine

Division name

Department of Endocrinology and Metabolism

Zip code


Address

5 Zaifu-cho, Hirosaki, Aomori-ken

TEL

0172-39-5062

Email

sannai@cc.hirosaki-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Murakami Hiroshi

Organization

Hirosaki University Graduate School of Medicine

Division name

Endocrinology and Metabolism

Zip code


Address

5 Zaifu-cho, Hirosaki, Aomori-ken

TEL

0172-39-5062

Homepage URL


Email

sannai@cc.hirosaki-u.ac.jp


Sponsor or person

Institute

A society for the study of SGLT2 in Aomori-ken

Institute

Department

Personal name



Funding Source

Organization

A society for the study of SGLT2 in Aomori-ken

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)

Astellas Pharma Inc.


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

青森県立中央病院糖尿病センター(青森県)、青森市民病院糖尿病・内分泌内科(青森県)、工藤内科クリニック(青森県)、村上病院糖尿病内科(青森県)、木村健一クリニック(青森県)、弘前市立病院内分泌代謝科(青森県)、黒石病院糖尿病・内分泌内科(青森県)、今村クリニック(青森県)、五日市内科医院(青森県)、八戸市民病院内分泌・糖尿病科(青森県)、青森労災病院糖尿病・内分泌内科(青森県)、中園内科クリニック(青森県)、向井田胃腸科内科(青森県)、大館市立総合病院糖尿病・内分泌・神経内科(秋田県)


Other administrative information

Date of disclosure of the study information

2014 Year 12 Month 15 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

Enrolling by invitation

Date of protocol fixation

2012 Year 11 Month 17 Day

Date of IRB


Anticipated trial start date

2014 Year 12 Month 15 Day

Last follow-up date

2016 Year 09 Month 30 Day

Date of closure to data entry

2016 Year 10 Month 31 Day

Date trial data considered complete

2016 Year 12 Month 31 Day

Date analysis concluded

2017 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2014 Year 12 Month 15 Day

Last modified on

2014 Year 12 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018559


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name