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Not yet recruitingNCT06683534Updated Apr 29, 2026

Palmitic Acid and Human Microvascular Function

A Phase 2 interventional study of Quercetin (dietary supplement) and Placebo in Microvascular Dysfunction, Microvasculature and Cardiovascular Diseases, sponsored by Medical College of Wisconsin. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-04-29.

Sponsored by Medical College of Wisconsin · Phase 2, Interventional, and Basic science

Phase
Phase 2
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Microvascular Dysfunction
  • Microvasculature
  • Cardiovascular Diseases
  • Cardiovascular Diseases (CVD)
  • Microvascular Health
  • Obesity and Overweight

Keywords

  • Obesity
  • Supplement
03

In context

Cardiovascular Diseases

4,905 studies on the registry are indexed under Cardiovascular Diseases; 919 are open to participants now.

This study's planned enrollment of 40 is below the median of 100 across 2,738 interventional studies indexed under Cardiovascular Diseases.

Browse Cardiovascular Diseases studies →

Lead sponsor

Medical College of Wisconsin is the lead sponsor of 540 studies on the registry; 119 are open to participants now.

Of its 71 completed or terminated interventional studies of FDA-regulated products, 56 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Obesity (BMI>30)
  • Aged 18-40 years
  • English Speaking

Exclusion criteria

Exclusion Criteria:

  • BMI>60
  • Resting SBP ≥180 mmHg or DBP ≥ 110mmHg
  • Pregnancy or breastfeeding.
  • Prior history of myocardial infarction
  • Diagnosis of more than 1 risk factor for coronary artery disease (active smoker, diabetes mellitus- type 1 or 2, congestive heart failure, hyperlipidemia, hypertension)
  • Active mouth sores that affect the buccal mucosa.
05

Study design

Phase
Phase 2
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Use of oral quercetin to improve human microvascular function

    Quercetin is a non-FDA approved, over-the-counter supplement that has been shown to improve oxidative capacity in blood vessels.

    Dietary Supplement: Quercetin (dietary supplement)

  • Placebo comparator
    Placebo

    A placebo will be administered for 30 days followed by assessment of the subject's microvascular function.

    Drug: Placebo

Interventions

  • Dietary supplementQuercetin (dietary supplement)

    Quercetin will be provided to take one Quercetin per day for 30 days to look for differences in microvascular function.

  • DrugPlacebo

    Subjects randomized to receive placebo will be administered a standard placebo sugar pill.

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: 2 hours

Secondary outcomes

  1. 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%).

    Time frame: 0.5 hours

07

Study locations

1 site
  • Froedtert Hospital
    Wauwatosa, Wisconsin 53226, United States
    • Julia Vogt · Contact · jvogt@mcw.edu · 4149552348
    • Julie Freed, MD, PhD · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06683534
Lead sponsor
Medical College of Wisconsin
Responsible party
Julie K. Freed (Executive Vice Chair, Medical College of Wisconsin) — Principal investigator
First posted
Nov 12, 2024
Start date
Jul 2026 (estimated)
Primary completion
Dec 2030 (estimated)
Completion
Dec 2030 (estimated)
Last update
Apr 29, 2026

Study contacts

Julia A Vogt
Contact
jvogt@mcw.edu
4149552348

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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