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Protease digested royal jelly pharmacokinetics study in healthy volunteers.

Not Applicable
Conditions
Adult
Registration Number
JPRN-UMIN000029627
Lead Sponsor
Yamada Bee Company, Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

The subjects in conflict with any of the following condition are excluded. 1) A person who has a food allergy 2) A person who has an asthma 3) A women who is pregnant, hope for the pregnancy, or breastfeeding 4) A parson who participated in other clinical trial at resent (past 3 months) 5) A person who has the infectious disease 6) A person with a history of the surgery considerable in the gastrointestinal tract site, for example, gastrectomy, stomach and intestines suturation, intestinal tract resection and so on. 7) A person who with the disease to liver, kidney, heart, diabetes and serious desease 8) A person who has received medical treatment of drug now 9) A person who can not visit the designated examination date (including the previous night) and be hospitalized until the trial end. 11) A person who Those who can not quit smoking from dinner the day before the examination to the examination end 12) A person who cannot take in royal jelly according to instruction or cannot maintain rest until the trial end. 13) A person who can not ban the intake of royal jelly-containing food from one week before the clinical trial. 14) A person who cannot keep regular hours 15) A person who is not daily service (who is night or rotation duty) 16) A person who has taken the blood sampling 200 mL within 4 weeks or 400 mL within 3 months at the time of starting this trial 17) A person who is a heavy alcohol drinker (over 500 mL beer per day ) 18) A person who is a heavy smorker (over 20 cigarettes per day) 19) A person who dentified as improper by the principal investigator or subinvestigators.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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