Clinical Trials Directory

Trials / Completed

CompletedNCT01957306

Safety and Efficacy of Dr. Tagliaferri's Menopause Formula

A Phase 2, Open Label Clinical Trial Assessing Safety and Efficacy of Dr. Tagliaferri's Menopause Formula for Hot Flushes and Menopausal Symptoms in Postmenopausal Women

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Herba Buena, Inc · Industry
Sex
Female
Age
40 Years – 65 Years
Healthy volunteers
Accepted

Summary

The primary goal of this study is to evaluate the safety and efficacy of 12 weeks of treatment of 4 grams/day of Dr. Tagliaferri's Menopause Formula (administered as 2 grams PO BID) in reducing the frequency of menopausal vasomotor symptoms among healthy, postmenopausal women, aged 40-65, with moderate to severe hot flushes.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTDr. Tagliaferri's Menopause FormulaAdministered as 2 grams PO BID

Timeline

Start date
2013-11-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2013-10-08
Last updated
2014-06-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01957306. Inclusion in this directory is not an endorsement.

Safety and Efficacy of Dr. Tagliaferri's Menopause Formula (NCT01957306) · Clinical Trials Directory