UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000059453
Receipt number R000067963
Scientific Title Tirzepatide's Assessment on Satiety and Treatment Experience
Date of disclosure of the study information 2025/10/20
Last modified on 2025/10/19 14:41:29

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Basic information

Public title

Tirzepatide's Assessment on Satiety and Treatment Experience

Acronym

TASTE study

Scientific Title

Tirzepatide's Assessment on Satiety and Treatment Experience

Scientific Title:Acronym

TASTE study

Region

Japan


Condition

Condition

type 2 diabetes mellitus

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

evaluating the impact on eating behavior of T2DM patient.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Changes in Eating Behavior Questionnaire before treatment and after six months.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

we prescribed self-injection 2.5 mg Tirzepatide per week. The prescribing physician will determine whether to increase the dose based on side effects and treatment efficacy at intervals of 4 weeks or longer, with the maximum increase being up to 15 mg per week.

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

75 years-old >=

Gender

Male and Female

Key inclusion criteria

T2DM patients who agreed on prescription of Tirzepatide

Key exclusion criteria

who disagreed Tirzepatide treatment

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Ryoichi
Middle name
Last name Ishibashi

Organization

Kimitsu Chuo Hospital

Division name

Department of Medicine, Division of Diabetes, Endocrinology and Metabolism

Zip code

292-8535

Address

1010 Sakurai, Kisarazu-City, Chiba 292-8535, Japan

TEL

0438-36-1071

Email

suzukiyasutaka009@gmail.com


Public contact

Name of contact person

1st name Ryoichi
Middle name
Last name Ishibashi

Organization

Kimitsu Chuo Hospital

Division name

Department of Medicine, Division of Diabetes, Endocrinology and Metabolism

Zip code

292-8535

Address

1010 Sakurai, Kisarazu-City, Chiba 292-8535, Japan

TEL

0438-36-1071

Homepage URL


Email

suzukiyasutaka009@gmail.com


Sponsor or person

Institute

Kimitsu Chuo 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

Kimitsu Chuo Hospital

Address

1010 Sakurai, Kisarazu-City, Chiba 292-8535, Japan

Tel

0438-36-1071

Email

suzukiyasutaka009@gmail.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

2025 Year 10 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

Enrolling by invitation

Date of protocol fixation

2023 Year 04 Month 01 Day

Date of IRB

2023 Year 11 Month 15 Day

Anticipated trial start date

2023 Year 05 Month 01 Day

Last follow-up date

2025 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 10 Month 19 Day

Last modified on

2025 Year 10 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067963