Completed

Phase 2
Age: 45Years - 55Years
FEMALE
NCT00000612

Soy Estrogen Alternative Study (SEA)

Led by National Heart, Lung, and Blood Institute (NHLBI) · Updated on 2016-05-13

N/A

Participants Needed

N/A

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To conduct a three-armed trial assessing the effect of soy phytoestrogens on menopausal complaints, plasma lipids and lipoproteins, vaginal bleeding and endometrial proliferation, and health related quality of life.

CONDITIONS

Official Title

Soy Estrogen Alternative Study (SEA)

Who Can Participate

Age: 45Years - 55Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

Perimenopausal/menopausal women, ages 45 to 55.

Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Site Locations not provided

Location information for this trial is currently unavailable.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

N/A

Primary Purpose

PREVENTION

Number of Arms

0

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Soy Estrogen Alternative Study (SEA) | DecenTrialz