An Exploratory Investigation of Dietary Supplementation and the Effect on Common Symptoms of Perimenopause and Menopause
NCT ID: NCT05617287
Last Updated: 2023-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
42 participants
INTERVENTIONAL
2022-09-03
2023-01-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Semaine Supplement
Participants are provided with a dietary supplement and are instructed to take 1 capsule per day. Participants are to take the supplement at the same time every day. If forgotten, they are to take it with the next meal. Participants will take a well-being assessment after each month (4 surveys total including the baseline.)
Semaine Menopause Supplement
Synergistic Dietary Supplement
Interventions
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Semaine Menopause Supplement
Synergistic Dietary Supplement
Eligibility Criteria
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Inclusion Criteria
* Moderate self-reported discomfort related to perimenopause or menopause. Participants will complete the menopause well-being survey and must answer an average of "moderate" or higher.
Exclusion Criteria
* Currently undergoing chemotherapy or has previously been treated for cancer
* Pregnancy, breastfeeding, or attempting to become pregnant during the study
* Known allergic reactions to components of the dietary supplement (red clover extract, olive extract, bergamot extract )
40 Years
57 Years
FEMALE
Yes
Sponsors
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Citruslabs
INDUSTRY
Semaine Health
INDUSTRY
Responsible Party
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Principal Investigators
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Christopher Hill
Role: PRINCIPAL_INVESTIGATOR
Citruslabs
Matthew Crane
Role: PRINCIPAL_INVESTIGATOR
Semaine Health
Locations
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Citruslabs
Santa Monica, California, United States
Countries
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Other Identifiers
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20265
Identifier Type: -
Identifier Source: org_study_id
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