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Burdock and Blood Pressure in African-American Women

Burdock and Blood Pressure in African-American Women: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02511860
Enrollment
60
Registered
2015-07-30
Start date
2015-08-31
Completion date
2016-02-29
Last updated
2015-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Brief summary

This is a study of women aged 18-65, to determine the physiological effects of consuming burdock root in supplement form. Burdock has long been used by herbalists for its diuretic and blood sugar lowering properties.

Detailed description

This study will allow us to determine the effect of burdock consumption on basic laboratory tests such as the complete metabolic panel (CMP) as well as the effect on blood pressure over time. Participants will self-monitor their blood pressures and undergo lab testing. They will also complete symptom inventories to determine subjective factors that change with burdock consumption, such as menstrual water retention. Subjects will undergo electronic body composition testing before and after the intervention.

Interventions

DIETARY_SUPPLEMENTBurdock

Subjects will consume burdock daily and will undergo laboratory tests to determine the effect of burdock, if any, on organ function.

DIETARY_SUPPLEMENTPlacebo

Methylcellulose (inert) tablet taken as placebo

Sponsors

Proactive Health Labs
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Must be able to swallow tablets * African-American race * Able to travel to our clinic in Santa Monica

Exclusion criteria

* Severely low blood pressure * Hypoglycemia * Baseline creatinine over 1.2

Design outcomes

Primary

MeasureTime frame
Blood pressure6 weeks

Secondary

MeasureTime frame
Extracellular/Total Body Water Ratio6 Weeks
Hemoglobin A1c6 weeks
Blood urea nitrogen6 weeks
Body fat percentage6 Weeks
Fasting Blood Glucose6 weeks
Liver function tests6 weeks
Creatinine6 weeks

Contacts

Primary ContactDr De
mde@phlabs.com3108995577

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026