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

NCT04228757 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2020-02-05

No results posted yet for this study

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.

Conditions

Interventions

DIETARY_SUPPLEMENT

phytoestrogen herbal blend

phytoestrogen herbal blend

OTHER

Placebo

Tablet without active ingredients

Sponsors & Collaborators

  • ObvioHealth

    collaborator INDUSTRY

  • i-Health, Inc.

    lead INDUSTRY

Principal Investigators

  • Parth Shah, MD · ObvioHealth

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-06-28
Primary Completion
2020-04-04
Completion
2020-04-04

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04228757 on ClinicalTrials.gov