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CompletedNCT07904832Updated Oct 29, 2026

Under Pressure: Arugula Extract's Effect on Blood Pressure in Hypertensive Individuals

An interventional study of Arugula Extract and Psyllium Husk in Hypertension (HTN) and Hypertension, sponsored by Baylor University. Completed at 1 site in United States. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Baylor University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 1 month after the study started (first participant enrolled Sep 2025, registered Oct 2026).
Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

The purpose of this randomized, single-blind, placebo-controlled, crossover study was to investigate the acute effects of arugula extract (AE) supplementation on blood pressure, endothelial function, and circulating nitric oxide (NO) metabolites in individuals with elevated to stage 1 hypertension. Hypertension is a major contributing factor to cardiovascular disease (CVD) and is commonly associated with endothelial dysfunction and impaired NO bioavailability. Dietary nitrate supplementation has demonstrated beneficial effects on cardiovascular health through the nitrate-nitrite-NO pathway. Although nitrate-rich supplements such as beetroot juice have been extensively investigated, limited research has examined the vascular effects of arugula extract in individuals with hypertension.

Sixteen adults between the ages of 18 and 50 years with elevated to stage 1 hypertension participated in the study. Participants completed two experimental conditions in randomized order: 4,000 mg of arugula extract, providing approximately 400 mg of dietary nitrate, and 4,000 mg of psyllium husk placebo. Each condition was separated by a minimum 72-hour washout period to minimize potential carryover effects.

During each experimental condition, participants underwent baseline cardiovascular and vascular assessments before consuming the assigned supplement. Systolic blood pressure, diastolic blood pressure, heart rate, and venous blood samples were collected at baseline and 1, 2, 3, and 24 hours following supplementation. Endothelial function was assessed through brachial artery flow-mediated dilation (FMD) at baseline, 3 hours, and 24 hours post-supplementation. Blood samples were analyzed to assess circulating nitrate, nitrite, and total NO metabolites.

The primary objective was to determine whether acute arugula extract supplementation improved endothelial function and reduced blood pressure compared with placebo. Secondary objectives included evaluating changes in circulating NO metabolites. This investigation sought to determine the potential of arugula extract as a dietary nitrate intervention for improving vascular health in individuals with elevated blood pressure.

02

Conditions studied

  • Hypertension (HTN)
  • Hypertension

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Keywords

  • Arugula
  • Hypertension
  • Vascular Health
  • Cardiovascular
03

In context

Hypertension

6,114 studies on the registry are indexed under Hypertension; 912 are open to participants now.

This study's enrollment of 16 is below the median of 100 across 4,575 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Baylor University is the lead sponsor of 42 studies on the registry; 9 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Males and females between the ages of 18 and 50
  • No previously diagnosed or known cardiovascular diseases aside from hypertension
  • Elevated or stage I hypertension in accordance to the AHA
  • Not Not currently taking any medication that may affect blood pressure, heart rate, or mental state (e.g., stimulants, anti-depressants, anti-anxiety)

Exclusion criteria

Exclusion Criteria:

  • >40 kg/m2
  • A blood pressure reading on two separate occasions indicating stage II hypertension according to the AHA.
  • Previously diagnosed with any cardiovascular or cardiometabolic disease (aside from hypertension)
  • Currently taking any prescription stimulants or anti-depressants
  • Taking any supplements with dietary nitrates (e.g., beet root juice, powder) or Nitric Oxide advertised supplements
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    Arugula Extract Followed by Placebo

    Participants in this arm will receive a single dose of 4,000 mg of arugula extract during the experimental condition, followed by a minimum 72-hour washout period. Participants subsequently receive a single oral dose of 4,000 mg psyllium husk (placebo) during the second experiential condition.

    Dietary Supplement: Arugula Extract

  • Experimental
    Placebo Followed by Arugula Extract

    Participants in this arm will receive a single dose of 4,000 mg of psyllium husk (placebo) during the experimental condition, followed by a minimum 72-hour washout period. Participants subsequently receive a single oral dose of 4,000 mg arugula extract during the second experiential condition.

    Dietary Supplement: Psyllium Husk

Interventions

  • Dietary supplementArugula Extract

    Participants consume a single oral dose of 4,000 mg arugula extract (AE), providing approximately 400 mg of dietary nitrate (10% nitrate concentration). Arugula Extract is administered in capsule form following baseline cardiovascular and vascular assessments. Blood pressure, heart rate, and blood biomarkers are assessed at baseline, 1, 2, 3, and 24 hours following supplementation. Flow-mediated dilation is assessed at baseline, 3 hours, and 24 hours.

  • Dietary supplementPsyllium Husk

    Participants consume a single oral dose of 4,000 mg psyllium husk as the placebo condition. The placebo is administered in capsule form following baseline cardiovascular and vascular assessments. Blood pressure, heart rate, and blood biomarkers are assessed at baseline, 1, 2, 3, and 24 hours following supplementation. Flow-mediated dilation is assessed at baseline, 3 hours, and 24 hours.

06

What researchers measure

Primary outcomes

  1. Endothelial Function

    Measured Via brachial artery flow-mediated dilation.

    Time frame: Baseline, 3-hours post supplementation, 24-hours post supplementation

  2. Blood Pressure

    Blood pressure will be measured using an automated oscillometric sphygmomanometer to determine systolic and diastolic blood pressure in mmHg.

    Time frame: Baseline, 1-hour post consumption , 2-hours post consumption, 3-hours post consumption, and 24-hours post consumption

  3. Biomarker of Nitric Oxide

    Nitrate and Nitrite are biomarkers of nitric oxide quantified through blood samples analysis. Measured with Enzyme-Linked Immunosorbent Assay (ELISA).

    Time frame: Baseline, 1-hour post consumption , 2-hours post consumption, 3-hours post consumption, and 24-hours post consumption

  4. Heart Rate

    Heart rate will be measured in conjunction with blood pressure using an automated oscillometric sphygmomanometer to determine beats per minute in bpm)

    Time frame: Baseline, 1-hour post consumption , 2-hours post consumption, 3-hours post consumption, and 24-hours post consumption

07

Study locations

1 site
  • Marrs Mclean Gym
    Waco, Texas 76706, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07904832
Lead sponsor
Baylor University
Responsible party
Sponsor
First posted
Oct 29, 2026
Start date
Sep 11, 2025
Primary completion
Jul 14, 2026
Completion
Jul 14, 2026
Last update
Oct 29, 2026

Oversight

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

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Studies of the drug tested here: Psyllium husk

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