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A Clinical Study Assessing Efficacy of an Herbal Blend on Menopausal Symptoms and Quality of Life

Menopause Clinical Trial

Official title:
A Clinical Study Assessing Efficacy of an Herbal Blend on Menopausal Symptoms and Quality of Life

Clinical Trial Summary

This 12-week study is a randomized, placebo-controlled study assessing the efficacy of an herbal blend on menopausal symptoms and quality of life.

Clinical Trial Description

The purpose of this study is to evaluate changes in menopause symptoms after taking an herbal supplement daily for 12 weeks compared to placebo (a tablet that does not have active ingredients). This is a remote study, meaning all study data will be collected via the ClaimIt app, with the exception of a screening lab appointment and a Week 12 lab appointment.Participants will be asked to report on study compliance and respond to a series of questionnaires relating to symptoms of menopause, hot flashes, and quality of life. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04228757
Study type Interventional
Source i-Health, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date June 28, 2019
Completion date April 4, 2020
View Details
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