Healthy adults
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: P-Participant: Participant The subjects were healthy adults (those who are not suffering from any diseases, excluding those under 18 years old, pregnant women, and lactating women) I-intervention: Intervention (food) characteristics Continuous intake of delphinidin 3,5-diglucoside, Unlimited dosage forms, period and follow-up period. C-Comparison: Comparison Placebo (The placebo's formulation is not specified) O-Outcome: Outcome The primary outcome: Tear secretion (Schirmer's test) The secondary outcome: Subjective symptoms (VAS, DEQS), Other eye-related indicators (pupillary response, tear break-up time, Flicker test) S-Study design: Study design Randomized parallel group controlled trials, randomized crossover trials, quasi-randomized parallel group controlled trials, quasi-randomized crossover trials, non-randomized parallel group controlled trials, non-randomized crossover trials or open trial
Exclusion criteria
Exclusion criteria: The literature which does not meet PICOS, such as conference abstracts (conference proceedings) that are not original articles will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tear secretion (Schirmer's test) | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjective symptoms (VAS, DEQS), Other eye-related indicators (pupillary response, tear break-up time, Flicker test) | — |
Countries
Japan
Contacts
Oryza Oil and Fat Chemical Co., Ltd. Planning & Solution Development Department Section