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Effect of a functional food "SNR-11" supplementation on unidentified complaints in premenopausal healthy women: A randomized, double-blind, and placebo-controlled trial

Effect of a functional food "SNR-11" supplementation on unidentified complaints in premenopausal healthy women: A randomized, double-blind, and placebo-controlled trial - Effect of a functional food "SNR-11" supplementation on unidentified complaints

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027691
Enrollment
70
Registered
2019-05-24
Start date
2017-08-01
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

Group A
1st phase: Oral intake of SNR-11, once a day for 7 days - washed out - 2nd phase: Oral intake of Placebo once a day for 7 days Group B
1st phase: Oral intake of Placebo, once a day for 7 days - washed out - 2nd phase: Oral intake of SNR-11 once a day for 7 days

Sponsors

Medical Co. LTA Fukuoka Mirai Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Premenopausal healthy women with normal menstrual cycle

Exclusion criteria

Exclusion criteria: Individuals who are allergic or intolerant to foods Individuals who have abnormalities to be enrolled Individuals who are or may be pregnant and nursing Individuals who are diagnosed inappropriate for the trial by the principal investigator

Design outcomes

Primary

MeasureTime frame
VAS values of unidentified complaints on day 6, 7, 8 of supplementation—

Countries

Japan

Contacts

Public ContactHiroshi Tsukikawa

Medical Co. LTA Fukuoka Mirai Hospital Clinical Research Center Planning and Coordination Dept

hiroshi-tsukikawa@lta-med.com092-662-3608

Outcome results

None listed

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