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Clinical Trials/JPRN-UMIN000045328
JPRN-UMIN000045328
Recruiting
未知

An exploratory study for relating the effect of test food on physical response to pollen environmental exposure - An exploratory study for relating the effect of test food on physical response to pollen environmental exposure

EP Mediate Co., Ltd.0 sites20 target enrollmentDecember 18, 2022
ConditionsHealthy adult

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy adult
Sponsor
EP Mediate Co., Ltd.
Enrollment
20
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 18, 2022
End Date
December 19, 2021
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\)Subjects having a disease requiring treatment or a history of serious diseases for which medication was required (2\)Subjects who get the vaccine last week before the Japanese cedar exposure and 4 days after the exposure (3\)Subjects who are treated with allergen immunotherapy for the Japanese cedar pollen (e.g. SLIT, SCIT etc.) or surgery of allergic rhinitis (e.g. laser surgery etc.) within the 3 year prior to the time of obtaining consent about participation in the study or plan them during the study (4\)Subjects who have acute rhinitis, nasal sinuses, hypertrophic rhinitis, or perennial allergy (5\)Subjects who are taking antiallergic drug (except from ointment) (6\)Subjects who received steroid medication (e.g. Kenacort\-A) within the 6 months prior to the time of obtaining consent (7\)Subject who having a habit of drinking coffee, Pu\-erh tea and Awa bancha tea more than 5 days a week (more than 100mL a day) (8\)Subjects who having possibilities for emerging allergy (9\)Subjects who intend to become pregnant (10\)Breastfeeding subjects (11\)Subjects who smoke excessively (more than 21 cigarettes a day) (12\)Subjects who regularly consume large amount of alcohol (having a drinking alcohol more than 5 days a week (\>\= 60g/day of alcohol) (13\)Subjects who have participated in other clinical study within the last three months at the time of obtaining consent (14\)Subjects judged as unsuitable for the study by the investigator for other reasons

Outcomes

Primary Outcomes

Not specified

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