UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000024817
Receipt number R000028565
Scientific Title Glucose excursions in patients with type 2 diabetes treated with mitiglinide/voglibose versus glimepiride: A randomized cross-over trial
Date of disclosure of the study information 2016/11/14
Last modified on 2017/01/25 16:33:16

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Basic information

Public title

Glucose excursions in patients with type 2 diabetes treated with mitiglinide/voglibose versus glimepiride: A randomized cross-over trial

Acronym

Glucose excursions with mitiglinide/voglibose versus glimepiride

Scientific Title

Glucose excursions in patients with type 2 diabetes treated with mitiglinide/voglibose versus glimepiride: A randomized cross-over trial

Scientific Title:Acronym

Glucose excursions with mitiglinide/voglibose versus glimepiride

Region

Japan


Condition

Condition

Type 2 diabetes

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate glucose excursions and the frequency of hypoglycemia in patients with type 2 diabetes treated with mitiglinide/voglibose versus glimepiride

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2


Developmental phase

Phase IV


Assessment

Primary outcomes

Glycemic excursions and the frequency of hypoglycemic evaluated using CGM on the last day of both periods

Key secondary outcomes

Metabolic profile changes during MTT


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

After receiving vildagliptin 100 mg, patients were randomized to have add-on therapy as either the fixed-dose combination drug mitiglinide/voglibose 10 mg/0.2 mg three times daily for a few days followed by glimepiride 1 mg once daily for several subsequent days

Interventions/Control_2

or vice versa

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

100 years-old >=

Gender

Male and Female

Key inclusion criteria

patients with type 2 diabetes who were taking DPP-4 inhibitors and were admitted to the general hospital for glycemic control

Key exclusion criteria

patients with insulin dependent diabetes; known allergies to mitiglinide, voglibose, or glimepiride; hepatic dysfunction; renal dysfunction; use of corticosteroids; existing pregnancy; alcoholism; a history of severe hypoglycemic episodes; a history of diabetic ketoacidosis; diabetic retinopathy with a high risk of hemorrhage

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kanta Fujimoto

Organization

Kobe City Medical Center General Hospital

Division name

Internal Medicine of Diabetes and Endocrinology

Zip code


Address

2-1-1 Minatojimaminamimachi, Chuo-ku, Kobe, Japan

TEL

075-302-4321

Email

kantachi@kcho.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kanta Fujimoto

Organization

Kobe City Medical Center General Hospital

Division name

Internal Medicine of Diabetes and Endocrinology

Zip code


Address

2-1-1 Minatojimaminamimachi, Chuo-ku, Kobe, Japan

TEL

075-302-4321

Homepage URL


Email

kantachi@kcho.jp


Sponsor or person

Institute

Kitano Hospital

Institute

Department

Personal name



Funding Source

Organization

none

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

北野病院(大阪府)


Other administrative information

Date of disclosure of the study information

2016 Year 11 Month 14 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

The mean glucose levels in the mitiglinide/voglibose and glimepiride groups were almost equal. the mitiglinide/voglibose group showed a significantly lower SD of glucose, MAGE, M-value, CONGA-1 value, and AUC >10 mmol/L than the glimepiride group. Hypoglycemia was not observed with mitiglinide/voglibose, whereas it was observed 0.35 times per day with glimepiride.

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 01 Month 01 Day

Date of IRB


Anticipated trial start date

2013 Year 04 Month 01 Day

Last follow-up date

2014 Year 10 Month 01 Day

Date of closure to data entry

2014 Year 10 Month 01 Day

Date trial data considered complete

2014 Year 10 Month 01 Day

Date analysis concluded

2014 Year 10 Month 01 Day


Other

Other related information



Management information

Registered date

2016 Year 11 Month 13 Day

Last modified on

2017 Year 01 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028565


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name