The purpose of this research is to study the effects of 12 weeks of melatonin supplementation compared to placebo in women who are in the menopause transition (perimenopause) and have high blood pressure.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
70
Participants will take SR melatonin 5mg (or placebo) orally 1 hour before bed, for approximately 12 weeks. The study is comparing the effects of melatonin supplementation vs. placebo on cardiovascular risk measures in perimenopausal women.
Participants will take SR melatonin 5mg (or placebo) orally 1 hour before bed, for approximately 12 weeks. The study is comparing the effects of melatonin supplementation vs. placebo on cardiovascular risk measures in perimenopausal women.
Mayo Clinic in Rochester
Rochester, Minnesota, United States
RECRUITINGChange in Nocturnal Systolic Blood Pressure (SBP)
Measured using 24-hour ambulatory blood pressure (ABP) monitoring, including nighttime BP levels and nocturnal BP dipping.
Time frame: Measured at baseline and at the end of the 12-week intervention
Change in Nocturnal Diastolic Blood Pressure (DBP)
Measured using 24-hour ambulatory blood pressure (ABP) monitoring, including nighttime BP levels and nocturnal BP dipping.
Time frame: Measured at baseline and at the end of the 12-week intervention.
Change in Oxidative Stress Markers
Assessed using Blood and urine samples analyzed by Mayo Clinic Laboratories.
Time frame: Measured at baseline and at the end of the 12-week intervention.
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