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CompletedNCT00119665

Clinical Trial Assessing Toxicity and Efficacy of MF101 for Hot Flashes

A Phase II, Double-Blind, Placebo-Controlled, Randomized Clinical Trial Assessing Toxicity and Efficacy of MF101 for Hot Flashes and Menopausal Symptoms

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
180 (planned)
Sponsor
Bionovo · Industry
Sex
Female
Age
40 Years – 60 Years
Healthy volunteers
Accepted

Summary

The researchers propose a Phase II randomized, double-blind, placebo-controlled trial of 180 healthy postmenopausal women experiencing at least 5 hot flashes per day or 35 hot flashes per week. Women will be randomized to one of three arms: 4.5 grams/day (dry weight of extract) of MF101, 9.0 grams/day (dry weight of extract) of MF101 or placebo for 12 weeks.

Conditions

Interventions

TypeNameDescription
DRUGMF101

Timeline

Start date
2006-02-01
Completion
2007-02-01
First posted
2005-07-14
Last updated
2007-05-17

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00119665. Inclusion in this directory is not an endorsement.

Clinical Trial Assessing Toxicity and Efficacy of MF101 for Hot Flashes (NCT00119665) · Clinical Trials Directory