common cold, influenza
Conditions
Interventions
Two groups: a group that gargled with granules containing UPs (UP group) and a group that gargled with granules not containing UPs (placebo group).
The 2 g/packet UP granules used in the present study
Sponsors
Wakayama University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Halthy volanteers
Exclusion criteria
Exclusion criteria: Those with serious somatic disorders including cerebrovascular disease, ischemic heart disease, cancer, and diabetes mellitus, and those who were pregnant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence and duration of common cold/influenza over the full 9-week trial period. The incidence and duration of common cold and influenza symptomatic days by week. | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence and duration of common cold and influenza symptoms(runny nose, sneezing, sore throat/throat discomfort (irritation), headache, cough, expectoration, fever, joint pain, and fatigue/malaise) over the full 9-week trial period. The incidence and duration of common cold and influenza symptoms by week. | — |
Countries
Japan
Contacts
Public ContactTakahiko Mitani
Wakayama University Research Center for Food and Agriculture
Outcome results
None listed