About this trial
The goal of this study is to learn how a supplement Quercetin can affect microvascular function.
Participants will:
* give two blood draws of 5 mL each * have a camera placed under the tongue to take pictures of blood vessels * have 2 laser Doppler microdialysis catheters placed on the forearm to monitor blood vessels before and after local drug infusion
Researchers will compare blood vessel function of those who take estrogen supplements to those who do not.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Obesity (BMI>30)
Aged 18-40 years
English Speaking
Disqualifiers
BMI>60
Resting SBP ≥180 mmHg or DBP ≥ 110mmHg
Pregnancy or breastfeeding.
Prior history of myocardial infarction
Trial design
Parallel
Treatments tested in this trial
Quercetin (dietary supplement)
Dietary supplementQuercetin will be provided to take one Quercetin per day for 30 days to look for differences in microvascular function.
Placebo
DrugSubjects randomized to receive placebo will be administered a standard placebo sugar pill.
Treatment groups
Trial outcomes
Primary outcomes
Change in blood vessel dilation
Peripheral microvascular dilation in response to acetylcholine, L-NAME, and sodium nitroprusside infusions will be measured using laser Doppler flowmetry with microdialysis.
Secondary outcomes
Change in Perfused Vessel Density
Total vessel density (TVD) will be calculated using the DeBacker Score manual analysis on all images that have a minimum microcirculation image quality score (MIQS) of 10. Perfused vessel density (PVD) will be calculated by multiplying total vessel density (TVD) x proportion of perfused vessels (PPV%).
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: