Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
Healthy Volunteers
ID07469475

Effect of a Daily Nitric Oxide-Stimulating Supplement on Plasma PAI-1 Levels: a Six-Week, Open-Label Clinical Trial

Led by University of California, Los Angeles · Updated on 2026-03-13

35

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the effects of a natural oral supplement on blood markers linked to vascular aging and inflammation in healthy adults. The study focuses on understanding how the supplement influences Plasminogen Activator Inhibitor-1 (PAI-1) and other proteins connected to cardiovascular risk and aging. This research aims to explore potential ways to support vascular health by enhancing nitric oxide production, which is important for blood vessel function and preventing clotting. Participants will take the oral supplement, which contains ginger extract, L-citrulline, Paullinia cupana, and muira puama, twice daily for six weeks. The study is open-label, meaning all enrolled participants receive the supplement without a comparison group or placebo. The trial will measure changes in several blood markers such as PAI-1, Interleukin-8, PCSK9, FGF-23, C-Reactive Protein, and Klotho, which are associated with inflammation, cardiovascular health, and aging. During the study, participants will have blood samples taken to assess these markers at the beginning and at the end of the six-week supplementation period. Blood pressure will also be monitored. Researchers will evaluate the change in these markers to understand how the supplement may affect vascular aging and inflammation. The total participation time covers the six weeks of supplement intake with assessments at baseline and treatment end.

CONDITIONS

Brief Title

Effect of a Daily Supplement on Plasma PAI-1 Levels

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • People of any gender at least 18 years of age who do not have a history of acute or chronic cardiovascular illnesses are eligible.
Not Eligible

You will not qualify if you...

  • Younger than 18 years of age
  • Currently pregnant (confirmed by pregnancy test for participants capable of pregnancy)
  • Using hormonal birth control
  • Current smoker
  • Allergy to ginger, muira puama, Paullinia cupana, or L-citrulline
  • Previous use of Revactin�AE or RM
  • History of serious cardiovascular events, including myocardial infarction (heart attack) or stroke
  • History of coronary, cardiac, or carotid surgery such as a stent, heart surgery, or endarterectomy
  • Active cancer of any type other than skin cancer

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants consume a daily oral supplement composed of ginger extract, L-citrulline, Paullinia cupana, and muira puama to study its effect on blood markers related to vascular aging and inflammation.

Twice daily supplement intake with visits for blood marker measurements at baseline and end of treatment

Trial Site Locations

Total: 2 locations

1

UCLA

Los Angeles, California, United States, 90034

Actively Recruiting

2

UCLA The Men's Clinic

Santa Monica, California, United States, 90403

Actively Recruiting

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Research Team

S

Sriram V Eleswarapu, MD, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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