A healthy male and female between 20 and 65 years old with a BMI of 25 or more and less than 30
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Candidate patients have to meet all the following inclusion criteria to participate in the study. (1) Male and female aged 20 to 65 years old at the time of acquisition (2) Persons whose BMI is 25 or more and less than 30 (3) A person who received a sufficient explanation about the examination, can understand the contents, obtains document consent by the principal
Exclusion criteria
Exclusion criteria: (1) Persons who regularly eat medicines, functional display foods, foods for specified health use, health foods, etc., which are likely to affect the test results (2) Those currently on a diet or planning to diet (3) Persons who are planning to travel on business with traveling during the examination period (4) Heavy alcohol drinkers (5) Persons with extremely irregular eating habits, those with irregular life rhythms (6) Persons who have a history of severe disease history and current medical history in the heart, liver, kidney and digestive organs (7) Persons with salinity limit (8) Those pregnant or planning pregnancy, and those who are breastfeeding (9) Participating in clinical trials of other medicinal products or health foods, within 4 weeks after completion of the study, or who plan to participate in other clinical trials after participating in the study (10) Persons conducting ongoing treatment with drugs (11) Persons who are allergic to pharmaceuticals and foods (in particular Nozawana pickled product) (12) Those who donated blood donated from the previous month or started donating 200 mL of whole blood (13) A man who donated 400 mL of whole blood three months before the start of the test (14) Women who donated 400 mL of whole blood from 4 months before the start of the test (15) A man who may donate more than 1,200 mL of whole blood from 12 months plus total blood draw amount of this test. (16) Women who may donate more than 800 mL of whole blood from 12 months plus total blood draw amount of this test. (17) Person who judged that participation in the examination is inappropriate by the investigator (medical doctor) or exam sharing physician
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of people who were able to eat 200 g of Nozawana pickled product (Nozawana Zuke) for 5 days / week or more | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in body weight, body mass index, body fat percentage and intestinal flora | — |
Countries
Japan
Contacts
CPCC Co., Ltd Clinical Research Planning Department