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NCT07469475 · ClinicalTrials.gov registry record · Phase 1

Effect of a Daily Supplement on Plasma PAI-1 Levels

A Phase 1 study of Aging and Endothelial Dysfunction, sponsored by University of California, Los Angeles.

Recruiting
Registry status
Phase 1
Development phase
35
Enrollment target
2
Study locations

NCT07469475 is a Phase 1 study of Aging and Endothelial Dysfunction that is actively recruiting participants, run by University of California, Los Angeles. The registered enrollment target is 35 participants, below the 2,195-participant average among 262 other Aging trials with a reported enrollment target (98% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT07469475, a Phase 1 study of Aging and Endothelial Dysfunction, is actively recruiting participants, sponsored by University of California, Los Angeles.

RECRUITING
Registry status
Phase 1
Development phase
35 participants
Enrollment target
2
Study locations

Study Summary

In a healthy person, the production of nitric oxide (NO) by the endothelium, the inner lining of the blood vessel, is responsible for a) the ability of the blood vessel to dilate so it can increase its blood flow and b) act as an anti-clotting product to prevent blood clotting in those vessels. Under physiological stress either due to the development of a disease such as diabetes or simply from aging, the endothelial cells can be impacted and become dysfunctional, thereby impairing their ability to make NO and even promoting the development of blood clots. When such endothelial dysfunction occurs, it may be a precursor for the future development of cardiovascular (CV) disease like hypertension or coronary artery disease later on in life in these patients. Therefore, the ability to enhance the local production or availability of NO within such affected blood vessels in patients identified as prone to endothelial dysfunction could play a positive role in either preventing or delaying the onset of endothelial dysfunction and subsequent CV disease in such patients. RM is an oral supplement consisting of natural ingredients and the amino acid, L-citrulline. In laboratory experiments with cells from the inner lining of blood vessels, the four components of RM have been shown to increase the concentration of NO and decrease the levels of some aging markers. In our recently completed study (manuscript currently in review), 31 young men and women took the supplement for 14 days and had no serious side effects. The supplement caused the expected potentially beneficial dilation of the blood vessels and decrease in the levels of Plasminogen Activator Inhibitor-1 (PAI-1), whose levels correlate with aging and risk of cardiovascular disease. In this study, healthy participants will consume the supplement for a 6-week period to determine if PAI-1 levels continue to be suppressed and also examine whether the supplement has an effect on other blood markers whose levels can change

Interventions

  • DIETARY_SUPPLEMENT Supplement with ginger extract, L-citrulline, Paullinia cupana, and muira puama

Study Locations (2)

California

  • UCLA - Los Angeles
  • UCLA The Men's Clinic - Santa Monica

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2026-02-24
Est. Completion 2026-12
Phase Phase 1

What the Registry Record Tells You About NCT07469475

The ClinicalTrials.gov registry entry for NCT07469475 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,195-participant average among 262 other Aging trials with a reported enrollment target (98% lower). The listed sponsor is University of California, Los Angeles, which has 897 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Aging appearing as the primary indexed condition, and to 1 intervention - of which Supplement with ginger extract, L-citrulline, Paullinia cupana, and muira puama is the first listed.

NCT07469475 reports 2 study locations spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT07469475 about?

NCT07469475 is a clinical study titled "Effect of a Daily Supplement on Plasma PAI-1 Levels". In a healthy person, the production of nitric oxide (NO) by the endothelium, the inner lining of the blood vessel, is responsible for a) the ability of the blood vessel to dilate so it can increase its blood flow and b) act as an anti-clotting product to prevent blood clotting in those vessels. Unde...

What is the current status of trial NCT07469475?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2026-02-24. Estimated completion is 2026-12.

What conditions does trial NCT07469475 study?

This clinical trial studies the following conditions: Aging, Endothelial Dysfunction, Senescence.

What interventions are being tested in trial NCT07469475?

The interventions under investigation include: Supplement with ginger extract, L-citrulline, Paullinia cupana, and muira puama (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT07469475?

This trial is sponsored by University of California, Los Angeles, which has 897 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07469475 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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