UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056804
Receipt number R000064923
Scientific Title Survey on the Intake of Oral Nutritional Supplements in Cancer Patients
Date of disclosure of the study information 2025/02/01
Last modified on 2025/04/09 11:01:29

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Basic information

Public title

Survey on the Intake of Oral Nutritional Supplements in Cancer Patients

Acronym

Survey on the Intake of Oral Nutritional Supplements in Cancer Patients

Scientific Title

Survey on the Intake of Oral Nutritional Supplements in Cancer Patients

Scientific Title:Acronym

Survey on the Intake of Oral Nutritional Supplements in Cancer Patients

Region

Japan


Condition

Condition

Cancer Patients

Classification by specialty

Hepato-biliary-pancreatic medicine Hepato-biliary-pancreatic surgery Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To deepen the understanding of the oral nutritional supplements required by cancer patients, and to assist in product development and appropriate product usage.

Basic objectives2

Others

Basic objectives -Others

None

Trial characteristics_1

Others

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

1. Background of the Study Participants (Age, Gender, Type of Cancer, Cancer Treatment, Presence of Appetite or Taste Disorders, and Oral Mucositis)
2. Feedback on Product A (Taste, Texture, Ease of Consumption, Intent to Continue Intake, and Willingness to Recommend to Others)

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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. Persons diagnosed with cancer
2. Aged 20 years or older
3. Those who have consumed Product A
4. Those who fully understand the research content and have provided voluntary consent to participate in this study
5. Capable of independently answering the survey

Key exclusion criteria

None

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Yukikazu
Middle name
Last name Kamada

Organization

Nestle Japan Ltd

Division name

Nestle Health Science Company

Zip code

140-0002

Address

Tennozu Ocean Square 20F, 2-2-20 Higashi-Shinagawa, Shinagawa-ku, Tokyo

TEL

070-2278-7597

Email

Yukikazu.Kamada@jp.nestle.com


Public contact

Name of contact person

1st name Hiroki
Middle name
Last name Takano

Organization

Nestle Japan Ltd

Division name

Nestle Health Science Company

Zip code

140-0002

Address

Tennozu Ocean Square 20F, 2-2-20 Higashi-Shinagawa, Shinagawa-ku, Tokyo

TEL

070-2448-5234

Homepage URL


Email

Hiroki.Takano@jp.nestle.com


Sponsor or person

Institute

Nestle Japan Ltd

Institute

Department

Personal name



Funding Source

Organization

Nestle Japan Ltd

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Shiba Palace Clinic Ethics Review Committee

Address

DaiwaA Hamamatsucho Bldg. 6F, 1-9-10, Hamamatsucho, Minato-ku, Tokyo, 105-0013, JAPAN

Tel

03-5408-1599

Email

shiba_palace@s-palace-clinic.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 02 Month 01 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

2025 Year 01 Month 21 Day

Date of IRB

2025 Year 01 Month 23 Day

Anticipated trial start date

2025 Year 02 Month 02 Day

Last follow-up date

2026 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2025 Year 01 Month 24 Day

Last modified on

2025 Year 04 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064923