UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018395
Receipt number R000021301
Scientific Title Prospective comparison of Luseogliflozin and alpha-glucosidase inhibitor on the management of diabetic patients with chronic heart failure and preserved left-ventricular ejection fraction
Date of disclosure of the study information 2015/09/20
Last modified on 2020/01/27 15:31:24

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Basic information

Public title

Prospective comparison of Luseogliflozin and alpha-glucosidase inhibitor on the management of diabetic patients with chronic heart failure and preserved left-ventricular ejection fraction

Acronym

Prospective comparison of Luseogliflozin and alpha-glucosidase inhibitor on the management of diabetic patients with chronic heart failure and preserved left-ventricular ejection fraction

Scientific Title

Prospective comparison of Luseogliflozin and alpha-glucosidase inhibitor on the management of diabetic patients with chronic heart failure and preserved left-ventricular ejection fraction

Scientific Title:Acronym

Prospective comparison of Luseogliflozin and alpha-glucosidase inhibitor on the management of diabetic patients with chronic heart failure and preserved left-ventricular ejection fraction

Region

Japan


Condition

Condition

heart failure

Classification by specialty

Cardiology Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effect of luseogliflozin on LV load in type 2 diabetic patients with heart failure with preserved ejection fraction compared to an alpha-glucosidase inhibitor, voglibose.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Change in BNP at 12 weeks

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

SGLT2 inhibitor, luseogliflozin
5 mg once a day

Interventions/Control_2

alpha-glucosidase inhibitor, voglibose
0.3mg three times/day

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

40 years-old <=

Age-upper limit

75 years-old >

Gender

Male and Female

Key inclusion criteria

1) Type 2 diabetic patients with LV ejection fraction > 45% and a symptom of heart failure
2) Inadequately controlled type 2 diabetic patients who have received alimentary therapy, exercise therapy, a lifestyle modification program, and hypoglycemic medications
3) Age >40 years and <75 years
4) Patients from whom a written informed consent was obtained

Key exclusion criteria

1) BNP <35 pg/ml
2) Patients receiving alpha-glucosidase inhibitors, SGLT2 inhibitors, glinides, high-dose sulfonylurea
3) Patients with renal insufficiency (eGFR< 30 ml/min/1.73m2)
4) LVEF<45%
5) Patients with history of severe ketoacidosis, diabetic coma within six months
6) Patients with serious infection and severe trauma, and perioperative patients
7) Type 1 diabetes mellitus
8) Poorly controlled type2 diabetic patients (HbA1c > 9.0%)
9) Uncontrolled hypertensive patients (systolic blood pressure >160mmHg)
10) Patients with history of stroke, myocardial infarction and severe cardiovascular disease with hospitalization within six months
11) Pregnant women and breast-feeding women
12) Patients with allergy for test drugs
13) Patients who is not suitable to this study due to medical reasons

Target sample size

190


Research contact person

Name of lead principal investigator

1st name Hiroshi
Middle name
Last name Ito

Organization

Okayama University Graduate School of. Medicine, Dentistry and Pharmaceutical Sciences

Division name

Cardiovascular Medicine

Zip code

700-8558

Address

2-5-1, Shikata-cho, Kita-ku, Okayama

TEL

086-235-7351

Email

itomd@md.okayama-u.ac.jp


Public contact

Name of contact person

1st name Toru
Middle name
Last name Miyoshi

Organization

Okayama University Graduate School of. Medicine, Dentistry and Pharmaceutical Sciences

Division name

Cardiovascular Medicine

Zip code

700-8558

Address

2-5-1 Shikada-cho Kita-ku Okayama

TEL

086-235-7351

Homepage URL


Email

miyoshit@cc.okayama-u.ac.jp


Sponsor or person

Institute

Cardiovascular Medicine
Okayama University Graduate School of. Medicine, Dentistry and Pharmaceutical Sciences

Institute

Department

Personal name



Funding Source

Organization

Novartis

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics committee of Okayama University

Address

2-5-1 Shikada-cho Kita-ku Okayama

Tel

086-235-6503

Email

mae6605@adm.okayama-u.ac.jp


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

2015 Year 09 Month 20 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

2015 Year 09 Month 30 Day

Date of IRB

2015 Year 09 Month 30 Day

Anticipated trial start date

2015 Year 10 Month 01 Day

Last follow-up date

2018 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 07 Month 23 Day

Last modified on

2020 Year 01 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021301


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name