Citrus depressa efficacy trial

Evaluate the anti-fatigue effect of intake of Citrus depressa: a randomized parallel group comparison study - Citrus depressa efficacy trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000037925

Enrollment

Registered

2019-09-10

Start date

2019-09-10

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adult

Interventions

Take a test article daily for 12 weeks Take a placebo daily for 12 weeks

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: BMI 23 or more and less than 30

Exclusion criteria

Exclusion criteria: 1. Subjects with food allergies 2. Subjects who are pregnant or lactating 3. Subjects who are judged as unsuitable for the study by the investigator for the other reason

Design outcomes

Primary

Measure	Time frame
blood test, urinalysis, subjective evaluation	—

Countries

Japan

Contacts

Public ContactTakeshi Kaneko

Japan Clinical Trial Association N.A.

info@yakujihou.org0364574666

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026