UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000057836
Receipt number R000066090
Scientific Title Sensory evaluation test for pet animals (dogs) of Sasa senanensis Rehder concentrated extract
Date of disclosure of the study information 2025/05/15
Last modified on 2025/05/13 16:59:51

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Basic information

Public title

Sensory evaluation test for pet animals (dogs) of Sasa senanensis Rehder concentrated extract

Acronym

Sensory evaluation test for pet animals (dogs) of Sasa senanensis Rehder concentrated extract

Scientific Title

Sensory evaluation test for pet animals (dogs) of Sasa senanensis Rehder concentrated extract

Scientific Title:Acronym

Sensory evaluation test for pet animals (dogs) of Sasa senanensis Rehder concentrated extract

Region

Japan


Condition

Condition

Dog owners

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The effects of oral intake of concentrated extract of Sasa senanensis on fecal odor, body odor, and breath odor of dogs are verified by sensory evaluation by owners. In addition, as a preliminary study, the effects on symptoms of periodontal disease are investigated.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Change from baseline in sensory evaluation

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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Oral intake of test food for 4 weeks

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

[Owner]
1) People who own healthy spayed or neutered dogs (male or female) between 1 and 10 years of age
2) People who can perform sensory evaluations during the evaluation period
3) People who are concerned about the fecal odor and/or body odor of the test animals
4) People who wish to participate in this study and have given written consent

Key exclusion criteria

[Dogs]
1) Case those have been taking medicines regularly for the past 3 months prior to the start of the study
2) Case those currently have a serious illness (diabetes, heart disease, liver disease, kidney disease, cancer, etc.)
3) Case those have a history of serious illness (diabetes, heart disease, liver disease, kidney disease, cancer, etc.) or digestive system disease
4) Case those have a medical abnormality during a health check or other examination within one year prior to obtaining consent
5) Case those regularly take food, supplements, etc. that may affect the study
6) Case those regularly take food, supplements, etc. that may affect the study during the study period and are unable to stop taking them during the study period
7) Case those are deemsd ineligible to participate in this study for any other reason by the principal investigator

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Miho
Middle name
Last name Kurone

Organization

Kurone clinic

Division name

Director

Zip code

206-0036

Address

25-6, Nakazawa2, Tama city, Tokyo, Japan

TEL

042-400-1092

Email

kur54981@gmail.com


Public contact

Name of contact person

1st name Miho
Middle name
Last name Kurone

Organization

Kurone clinic

Division name

Director

Zip code

206-0036

Address

25-6, Nakazawa2, Tama city, Tokyo, Japan

TEL

042-400-1092

Homepage URL


Email

kur54981@gmail.com


Sponsor or person

Institute

Kanamori Giken Co., Ltd

Institute

Department

Personal name



Funding Source

Organization

Self-Procurement

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

Ethics Review Committee of Watanabe Hospital

Address

5-16, Haneda1, Ota-ku, Tokyo, Japan

Tel

03-3741-0223

Email

wnb@cto-net.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

2025 Year 05 Month 15 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

Preinitiation

Date of protocol fixation

2025 Year 05 Month 07 Day

Date of IRB


Anticipated trial start date

2025 Year 07 Month 01 Day

Last follow-up date

2025 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

2025 Year 05 Month 12 Day

Last modified on

2025 Year 05 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066090