UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051349
Receipt number R000058583
Scientific Title Efficacy of once-weekly Semaglutide 1mg versus once-weekly Tirzepatide on glycemic control measured by continuous glucose monitoring in adults with type 2 diabetes
Date of disclosure of the study information 2023/06/20
Last modified on 2024/03/29 10:46:55

* 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

Efficacy of once-weekly Semaglutide 1mg versus once-weekly Tirzepatide on glycemic control measured by continuous glucose monitoring in adults with type 2 diabetes

Acronym

Efficacy of once-weekly Semaglutide 1mg versus once-weekly Tirzepatide on glycemic control measured by continuous glucose monitoring in adults with type 2 diabetes

Scientific Title

Efficacy of once-weekly Semaglutide 1mg versus once-weekly Tirzepatide on glycemic control measured by continuous glucose monitoring in adults with type 2 diabetes

Scientific Title:Acronym

Efficacy of once-weekly Semaglutide 1mg versus once-weekly Tirzepatide on glycemic control measured by continuous glucose monitoring in adults with type 2 diabetes

Region

Japan


Condition

Condition

Type 2 Diabetes

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Verification of superiority of Time In Range at Week 24

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Proportion of Time In Range at Week 24

Key secondary outcomes

Proportion of Time In Tight Range at Week 24.
Others of Glycemic indicator(MAGE,CV,MODD,CONGA2,IQR)
Change in body composition from baseline to week 24(Muscle mass, body fat mass, lean body mass, body water mass, skeletal muscle mass index)


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

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Once-weekly Semaglutide 1mg

Interventions/Control_2

Once-Weekly Tirzepatide(Doze escalation)

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

Type 2 diabetes over 20 years old
Patients who have been treated with Semaglutide 1mg
Patients with HbA1c 6.5% or more and less than 10.5%
Patients with BMI 22kg/m2 or more

Key exclusion criteria

Patients diagnosed with type 1 diabetes
Patients with a history of chronic pancreatitis or acute pancreatitis
Patients with severe infections
Patients in need of surgery
Other patients deemed inappropriate by the physician

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Yasutake
Middle name
Last name Shinohara

Organization

Tochigi Medical Center Shimotsuga

Division name

Diabetes and Endocrinology

Zip code

329-4498

Address

420-1Kawatsure,Ohira-machi,Tochigi -city,Japan

TEL

0282-22-2551

Email

yasutake@dokkyomed.ac.jp


Public contact

Name of contact person

1st name Yasutake
Middle name
Last name Shinohara

Organization

Tochigi Medical Center Shimotsuga

Division name

Diabetes and Endocrinology

Zip code

329-4498

Address

420-1Kawatsure,Ohira-machi,Tochigi -city,Japan

TEL

0282-22-2551

Homepage URL


Email

yasutake@dokkyomed.ac.jp


Sponsor or person

Institute

Tochigi Medical Center Shimotsuga

Institute

Department

Personal name



Funding Source

Organization

NONE

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

Tochigi Medical Center Shimotsuga

Address

420-1Kawatsure,Ohira-machi,Tochigi -city,Japan

Tel

0282-22-2551

Email

yasutake@dokkyomed.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

2023 Year 06 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

Terminated

Date of protocol fixation

2023 Year 04 Month 23 Day

Date of IRB

2023 Year 05 Month 24 Day

Anticipated trial start date

2023 Year 06 Month 20 Day

Last follow-up date

2024 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

2023 Year 06 Month 15 Day

Last modified on

2024 Year 03 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058583


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name