UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037603
Receipt number R000042875
Scientific Title Long-term efficacy and safety of the GLP-1 receptor agonist liraglutide in Japanese patients with type 2 diabetes mellitus.
Date of disclosure of the study information 2019/08/06
Last modified on 2019/11/25 14:27:01

* 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

Long-term efficacy and safety of the GLP-1 receptor agonist liraglutide in Japanese patients with type 2 diabetes mellitus.

Acronym

Long-term efficacy and safety of the GLP-1 receptor agonist liraglutide in Japanese patients with type 2 diabetes mellitus.

Scientific Title

Long-term efficacy and safety of the GLP-1 receptor agonist liraglutide in Japanese patients with type 2 diabetes mellitus.

Scientific Title:Acronym

Long-term efficacy and safety of the GLP-1 receptor agonist liraglutide in Japanese patients with type 2 diabetes mellitus.

Region

Japan


Condition

Condition

Type 2 Diabetes mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We retrospectively evaluated the long-term efficacy and safety of the GLP-1 receptor agonist liraglutide in Japanese patients with type 2 diabetes mellitus.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

The change in the eGFR slope and urine albumin creatinine ratio

Key secondary outcomes

Metabolic marker; HbA1c and body weight
Hemodynamic marker; systolic and diastolic blood pressure, and heart rate
Liver enzyme marker; AST, ALT and gamma-GTP
Liver fibrosis marker; Fib-4 index
Arteriosclerosis marker; IMT and PWV
Safety marker; incidence rate of Hypoglycemia


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Type 2 diabetes
Administration of liraglutide

Key exclusion criteria

Participation in the study is judged by the investigator or sub-investigator as inappropriate for any other reason

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name Takeshi
Middle name
Last name Osonoi

Organization

Nakakinen clinic

Division name

Director

Zip code

311-0113

Address

745-5 Nakadai, Naka-shi, Ibaraki

TEL

029-353-2800

Email

t-osonoi@kensei-kai.com


Public contact

Name of contact person

1st name Kensuke
Middle name
Last name Ofuchi

Organization

Nakakinen clinic

Division name

Department of clinical research

Zip code

311-0113

Address

745-5 Nakadai, Naka-shi, Ibaraki

TEL

029-353-2800

Homepage URL


Email

k-ofuchi@kensei-kai.com


Sponsor or person

Institute

Nakakinen clinic

Institute

Department

Personal name



Funding Source

Organization

Self-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

Nakakinen clinic

Address

745-5 Nakadai, Naka-shi, Ibaraki

Tel

029-353-2800

Email

k-ofuchi@kensei-kai.com


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

2019 Year 08 Month 06 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

1000

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

2019 Year 04 Month 26 Day

Date of IRB

2019 Year 05 Month 29 Day

Anticipated trial start date

2019 Year 05 Month 31 Day

Last follow-up date

2019 Year 06 Month 30 Day

Date of closure to data entry

2019 Year 06 Month 30 Day

Date trial data considered complete

2019 Year 06 Month 30 Day

Date analysis concluded

2019 Year 06 Month 30 Day


Other

Other related information

Single facility retrospective observation study


Management information

Registered date

2019 Year 08 Month 06 Day

Last modified on

2019 Year 11 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042875


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name