Completed
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
Eligibility Criteria
You may qualify if you...
Perimenopausal/menopausal women, ages 45 to 55.
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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