UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010999
Receipt number R000012849
Scientific Title The efficacy of teneligliptin in diabetic patients on hemodialysis
Date of disclosure of the study information 2013/06/24
Last modified on 2015/10/07 09:37:44

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Basic information

Public title

The efficacy of teneligliptin in diabetic patients on hemodialysis

Acronym

The efficacy of teneligliptin in diabetic patients on hemodialysis

Scientific Title

The efficacy of teneligliptin in diabetic patients on hemodialysis

Scientific Title:Acronym

The efficacy of teneligliptin in diabetic patients on hemodialysis

Region

Japan


Condition

Condition

Type2 diabetic patients on hemodialysis

Classification by specialty

Endocrinology and Metabolism Nephrology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To assess the efficacy and the safety of teneligliptin in type2 diabetic patients on hemodialysis

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase IV


Assessment

Primary outcomes

The primary end-point is postprandial plasma glucose, glycated albumin or HbA1c measurement three months after new, additional administration of teneligliptin and change from alogliptin in type 2 diabetic patients on hemodialysis.

Key secondary outcomes

Other laboratory data, hemodialytic indices and adverse events will be analyzed as well.


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

1) Fresh cases for DPP-4 inhibitor:
Patients with poor glycemic control (HbA1c level exceeding 7.0% and/or glycated albumin level exceeding 21.0%) after two months on conventional therapy (dietary therapy alone or mitiglinide and/or alpha-glucosidase inhibitor).
2) Cases whose treatment is changed from other DPP-4 inhibitors:
Patients have been treated with alogliptin.

Key exclusion criteria

Patients having infectious diseases, thyroid disease, or malignant tumors. Patients being treated with steroids.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Machiko Komatsu

Organization

Kawashima Hospital

Division name

Department of diabetes mellitus

Zip code


Address

1-1-39 Kitasako, Tokushima, 770-8548, Japan

TEL

088-631-0110

Email

machikomatsu@r7.dion.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Akiko Miyajima

Organization

Kawashima Hospital

Division name

The general affairs division

Zip code


Address

1-1-39 Kitasako, Tokushima, 770-8548, Japan

TEL

088-631-0110

Homepage URL


Email

a.miyajima@khg.or.jp


Sponsor or person

Institute

Kawashima Hospital

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

None


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 06 Month 24 Day


Related information

URL releasing protocol


Publication of results

Published


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 06 Month 03 Day

Date of IRB


Anticipated trial start date

2013 Year 06 Month 24 Day

Last follow-up date

2016 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

To evaluate the efficacy and the safety of teneligliptin in type 2 diabetic patients on hemodialysis


Management information

Registered date

2013 Year 06 Month 19 Day

Last modified on

2015 Year 10 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000012849


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name