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Name:
UMIN ID:

Recruitment status No longer recruiting
Unique ID issued by UMIN UMIN000027791
Receipt No. R000031843
Scientific Title A study for the effects of ingestion of yogurt in adults with discomfort of eyes and nose :A randomized, double-blind, placebo controlled trial
Date of disclosure of the study information 2018/12/23
Last modified on 2018/10/22

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Basic information
Public title A study for the effects of ingestion of
yogurt in adults with discomfort of eyes and nose :A randomized, double-blind, placebo controlled trial
Acronym A study for the effects of ingestion of
yogurt in adults with discomfort of eyes and nose
Scientific Title A study for the effects of ingestion of
yogurt in adults with discomfort of eyes and nose :A randomized, double-blind, placebo controlled trial
Scientific Title:Acronym A study for the effects of ingestion of
yogurt in adults with discomfort of eyes and nose
Region
Japan

Condition
Condition Healthy adults
Classification by specialty
Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 This study aims to evaluate the effects of ingestion of yogurt on the subjective evaluation of the discomfort of eyes and nose, and blood index
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Questionnaire of discomfort of eyes and nose,Diary.
Evaluate at points of 12-week and 4-week, 8-week
Key secondary outcomes Specific IgE(RAST), IFN-Gamma, IL-13, Total IgE(RIST)


Base
Study type Interventional

Study design
Basic design Parallel
Randomization Randomized
Randomization unit Individual
Blinding Double blind -all involved are blinded
Control Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 2
Purpose of intervention Prevention
Type of intervention
Food
Interventions/Control_1 Ingestion of yogurt drink containing lactic acid bacteria LH strain for 12 consecutive weeks
Interventions/Control_2 Ingestion of yogurt drink without lactic acid bacteria LH strain for 12 consecutive weeks
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
64 years-old >=
Gender Male and Female
Key inclusion criteria (1)Subjects aged from 20 to 64 years old
(2)Subjects with discomfort of eyes and nose(sneeze,runny nose, nasal)
(3)Subjects positive for specific IgE(RAST)against house dust or mite.
(4)Subjects who are judged as healthy adult for the study by the investigator
Key exclusion criteria (1)Subjects who routinely take foods or medicines containing of lactic acid bacteria.
(2)Subjects who routinely take foods or medicines affecting the test result
(3)Subjects who have history of
regular visits of otorhinolaryngology or planned to clinic visits
(4)Subjects who has received a diagnosis of seasonal allergic rhinitis (pollen allergy)
(5)Subjects with acute rhinitis, sinusitis or hypertrophic rhinitis
(6)Subjects with bronchial asthma
(7)Subjects who are under treatment or have a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease)
(8)Subjects who are under medication(e.g., hyposensitization)which may influence the outcome of the study
(9)Subjects with allergies to the test food in the study
(10)Subjects judged as unsuitable for the study by the investigator for laboratory evidence or cardiopulmonary function
(11)Subjects who have a disease requiring regular medication or a history of serious diseases for which medication was required
(12)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination
(13)Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study
(14)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating
(15)Subjects who are judges as unsuitable for the study based on the results of lifestyle questionnaire
(16)Subjects who are judged as unsuitable for the study by the investigator for other reason
Target sample size 100

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Takashi Fujta
Organization MEGMILK SNOW BRAND Co.,Ltd.
Division name Milk Science Research Institute. Food Function Laboratory
Zip code
Address 1-1-2 Minamidai,Kawagoe,Saitama,Japan
TEL 049-242-8111
Email tfujita@meg-snow.com

Public contact
Name of contact person
1st name
Middle name
Last name Chiharu Goto
Organization TTC Co., Ltd.
Division name Clinical Research Planning Department
Zip code
Address 1-20-2, Ebisunishi, Shibuya-ku, Tokyo
TEL 03-5459-5329
Homepage URL
Email c.goto@ttc-tokyo.co.jp

Sponsor
Institute TTC Co., Ltd.
Institute
Department

Funding Source
Organization MEGMILK SNOW BRAND Co.,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
Address
Tel
Email

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
2018 Year 12 Month 23 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 No longer recruiting
Date of protocol fixation
2017 Year 06 Month 08 Day
Date of IRB
Anticipated trial start date
2017 Year 06 Month 18 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information

Management information
Registered date
2017 Year 06 Month 16 Day
Last modified on
2018 Year 10 Month 22 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031843

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


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