Effects of Phytoestrogen From Pueraria Mirifica in Improvement of Serum Lipid Parameters in Postmenopausal Women
Dhurakij Pundit University
10 participants
Mar 2, 2024
INTERVENTIONAL
Conditions
Summary
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
Eligibility
Inclusion Criteria7
- Natural menopause, last menstrual period more than one year ago.
- Abnormal lipid profile parameters The criteria set for this research are:
- LDL\>130 mg/Dl or
- TG\>150 mg/Dl or
- Total cholesterol\>200 mg/Dl or
- HDL-C less than 50 mg/Dl. (Latest blood results not more than 6 months)
- Willing to participate in the project
Exclusion Criteria10
- Have ever received lipid-lowering medication or hormone replacement therapy or SERMs. During the past 6 weeks
- have had surgery on the ovaries or uterus before
- have a history of cancer within a 5-year period
- have diabetes or uncontrolled high blood pressure, including HbA1c \>9, Systolic blood pressure \>180 or Diastolic blood pressure \>110
- Endocrine system disease such as thyroid
- Ever had an organ transplant
- Regularly use drugs, marijuana, or drink alcohol.
- has a psychiatric disorder
- have other serious medical conditions that require close monitoring
- Inconvenient to follow up until the end of the research.
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Interventions
consume 1 capsule twice a day for 2 months which one capsule composed of dry weight 50 mg of Pueraria Mirifica 1or Pueraria Mirifica 2 or Pueraria Mirifica 3
Diet control \& life style modification
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06220266