UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012533
Receipt number R000014669
Scientific Title The effect of anagliptin on blood glucose and lipid levels in type 2 diabetes mellius
Date of disclosure of the study information 2013/12/09
Last modified on 2017/06/13 10:22:23

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

The effect of anagliptin on blood glucose and lipid levels in type 2 diabetes mellius

Acronym

The hypoglycemic and lipidemic effect of anagliptin in type 2 diabetes mellius

Scientific Title

The effect of anagliptin on blood glucose and lipid levels in type 2 diabetes mellius

Scientific Title:Acronym

The hypoglycemic and lipidemic effect of anagliptin in type 2 diabetes mellius

Region

Japan


Condition

Condition

Type 2 diabetes mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to investigate the effect of anagliptin on glycemic control and safty in patients with type 2 diabetes.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase



Assessment

Primary outcomes

Change of HbA1c and lipid levels

Key secondary outcomes

1) Achiemement rate of blood glucose <130mg/dl
2) The change of glycemic and lipid parameters.
3)The analysis of backgorund factors which affect glycemic and lipid control


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

85 years-old >

Gender

Male and Female

Key inclusion criteria

1)before test registration -anagliptin within 2 weeks outpatient
2)Type 2 diabetes
3)HbA1c :more than 7.0%, less than 9%
4)No plan to add other OHA
5)Age more than 20, less than 85
6)Patients with written IC

Key exclusion criteria

1)Allergy for vildagliptin, linagliptin, repaglinide and glimepiride
severe infection, before operation, severe trauma
2)severe ketosis, diabetic coma within 6 months
3)severe hepatic dysfunction or severe renal dysfunction (SCr:more than 2.0mg/dl or eGFR less than 30)
4)pregnacy
5)Patients judged by the investigator to be ineligible for some other reason

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Tadashi Yamakawa

Organization

Yokohama City University Medical Center

Division name

Department of Endocrinology and Diabetes

Zip code


Address

4-57 Urafune-cho, Minami-ku, Yokohama City, 232-0024, Japan

TEL

045-261-5656

Email

naibunpi@urahp.yokohama-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Tadashi Yamakawa

Organization

Yokohama City University Medical Center

Division name

Department of Endocrinology and Diabetes

Zip code


Address

4-57 Urafune-cho, Minami-ku, Yokohama City, 232-0024, Japan

TEL

045-261-5656

Homepage URL


Email

naibunpi@urahp.yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama City University Medical Center

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

JAPAN


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

2013 Year 12 Month 09 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

2013 Year 07 Month 11 Day

Date of IRB


Anticipated trial start date

2013 Year 12 Month 09 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The purpose of this study is to investigate the effect of anagliptin on glycemic control and safty in patients with type 2 diabetes.


Management information

Registered date

2013 Year 12 Month 09 Day

Last modified on

2017 Year 06 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014669


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name