Skip to content

Evaluation of the effect of flaxseed lignan on menopausal symptoms

Evaluation of the effect of flaxseed lignan on menopausal symptoms - Evaluation of the effect of flaxseed lignan on menopausal symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000047557
Enrollment
150
Registered
2022-06-19
Start date
2022-06-14
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 person

Interventions

Secoisolariciresinol diglucoside (SDG) low dose capsule (2 capsules per day) Secoisolariciresinol diglucoside (SDG) high dose capsule (2 capsules per day) Placebo food (2 capsules per day)

Sponsors

Macromill, Inc.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Females between the ages of 35-60 years at the time of consent. (2) Those who are able to consume the test meal continuously. (3) Those who are in the transitional period (less than 3 years from the last menstrual period) or after menopause (less than 3 years from the last menstrual period). (4) Those who have subjective symptoms related to menopause (5) Simplified Menopausal Index (SMI): 26 points or more. (6) Those who can avoid binge drinking and excessive exercise during the study period and lead the same lifestyle (diet, exercise, etc.) as before the study period. (7) Those who have received sufficient explanation of the purpose and content of this study, have the ability to consent, and can voluntarily volunteer to participate with a good understanding of the study, and agree to participate in this study in writing. (8) Those who receive no medication.

Exclusion criteria

Exclusion criteria: (1) Those who have food allergy. (2) Those who are pregnant or lactating, or plan to become pregnant or lactate during the study. (3) Those who have participated in other clinical studies within 3 months of consent and those who plan to participate in other clinical studies during the study period. (4) Those who have undergone oophorectomy or hysterectomy. (5) Those with extremely irregular diets or irregular sleep rhythms (e.g., Night and day shift worker). (6) Those who regularly use medicines, food for specified health use, functional food, or health food that may affect the evaluation items. (7) Those who have been taking hormone therapy. (8) Those who excessively smoke or excessively consume alcohol. (9) Those who are undergoing treatment for a disease, or have a history of a serious disease that required medication. (10) Patients with serious diseases such as diabetes, hepatic disease, renal disease, or cardiac disease, or those with a history of such diseases. (11) Those who are judged to be inappropriate as subjects based on the answers to various questionnaires. (12) Others, who are judged by the principal investigator to be inappropriate as subjects.

Design outcomes

Primary

MeasureTime frame
The simplified menopausal index (SMI) test

Secondary

MeasureTime frame
Questionnaires related to menopausal symptoms

Countries

Japan

Contacts

Public ContactTadashi Nishikawara

Macromill, Inc. Secretariat "Evaluation test for menopausal symptom improvement by flax lignan

monitor@terra-k.co.jp0120-998-017

Outcome results

None listed

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