Actively Recruiting
Effects of Phytoestrogen From Pueraria Mirifica in Improvement of Serum Lipid Parameters in Postmenopausal Women
Led by Dhurakij Pundit University · Updated on 2024-05-24
10
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn about the effects of phytoestrogen from Pueraria Mirifica in improvement of serum lipid parameters. The primary question it aims to answer are: • phytoestrogen from Pueraria Mirifica can reduce serum triglyceride, total cholesterol, LDL and increase HDL or not Participants will receive capsules which composed of dry weight 50 mg of Pueraria Mirifica twice a day for 2 months. Researchers will compare with diet control\&life style modification to see if there is the improvement of serum lipid parameters
CONDITIONS
Official Title
Effects of Phytoestrogen From Pueraria Mirifica in Improvement of Serum Lipid Parameters in Postmenopausal Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Natural menopause with last menstrual period more than one year ago
- Abnormal lipid profile with at least one of the following: LDL >130 mg/dL, triglycerides >150 mg/dL, total cholesterol >200 mg/dL, or HDL cholesterol less than 50 mg/dL based on blood tests within the last 6 months
- Willingness to participate in the study
You will not qualify if you...
- Use of lipid-lowering medication, hormone replacement therapy, or selective estrogen receptor modulators within the past 6 weeks
- Previous surgery on ovaries or uterus
- History of cancer within the past 5 years
- Diabetes or uncontrolled high blood pressure (HbA1c >9, systolic >180 mmHg, diastolic >110 mmHg)
- Endocrine diseases such as thyroid disorders
- History of organ transplant
- Regular use of drugs, marijuana, or alcohol
- Psychiatric disorders
- Serious medical conditions requiring close monitoring
- Unable or unwilling to follow up until the end of the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Dhurakij Pundit University
Laksi, Bangkok, Thailand, 10210
Actively Recruiting
Research Team
P
Prischa Saengow, MD.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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