Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05595915
Other study ID # IRB: 22-001158
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date June 1, 2023
Est. completion date November 30, 2023

Study information

Verified date June 2023
Source University of California, Los Angeles
Contact Sriram V. Eleswarapu, MD, PhD
Phone 3107943058
Email seleswarapu@mednet.ucla.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In a young and 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 promote 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 even coronary artery disease later on in life in these patients. Therefore, the ability to somehow 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. COMP-4 is a safe, clinically available, well tolerated oral supplement that has been shown in the lab to increase NO production in a number of differing tissues including human vascular endothelial cells. In this proposed human study, the investigators plan on recruiting healthy, young participants willing to take COMP-4 for a 14 day period in whom the investigators will measure in a non-invasive way - by the use of ultrasound - the effect of COMP-4 on its ability to improve blood flow in one of the major blood vessels of the upper arm. In addition, the investigators will also determine whether COMP-4 will be capable of lowering in the blood the levels of two of the most studied inflammatory markers associated with endothelial dysfunction, IL-8 and PAI-1.


Description:

The endothelium is the innermost layer of the blood vessel. It is composed of cells that produce nitric oxide (NO), a molecule required for normal endothelial function which includes vascular dilatation, platelet aggregation and protection of the vessel against injuries. Endothelial dysfunction (EnD), on the other hand, is defined as an inadequate production and/or release of NO from the vascular endothelium that can result in a) an impairment in vasodilation, b) migration and proliferation of the vascular smooth muscle cells, and c) promotion of thrombosis due to platelet aggregation. When present, EnD has been heralded as an early event for the development of cardiovascular disease. IL-8 and PAI-1 are two inflammatory markers that rise in the blood when EnD is present. In addition, flow mediated dilation (FMD), a validated non-invasive test to measure vasodilator function of the peripheral vasculature, is a commonly used method for assessment of EnD. NO is produced by a family of enzymes called nitric oxide synthases (NOS) that uses L-arginine to produce NO. Normally, the isozyme of NOS within the endothelium of the blood vessels that produces NO is called endothelial NOS (eNOS). However, NO is also produced during times of stress by the cells themselves to protect against oxidative damage and cell dysfunction. The NO that is induced in such a scenario is synthesized by the inducible NOS (iNOS) isozyme which is upregulated during times of stress to produce NO for its protective anti-oxidative effects. COMP-4 is an available oral supplement that combines three naturally occurring products: ginger, muira puama, and Paullinia cupana as well as the amino acid, L-citrulline. COMP-4 has been studied in the corporal smooth muscle cells (CSMC) of both humans and rats as well as in the osteoblast of the rat. In the CSMC, the increase in NO from iNOS induction by COMP-4 decreases local oxidative stress, reverses aging related corporal fibrosis and improves erectile function. With respect to the osteoblast, COMP-4 has been shown to stimulate NO not only from iNOS induction but also from upregulating eNOS by the osteoblast which has led to an enhancement in the healing of bone fractures as well as preventing the development of osteoporosis following ovariectomy. Preliminary unpublished studies in a human umbilical arterial endothelial cell line suggest that COMP-4 is also capable of stimulating the production of NO de novo from these endothelial cells. COMP-4 itself, in an initially published 3-month pilot study in men, has been shown to have no to minimal side effects and this side effect profile has borne out since it became available to the public about 5 years ago and has been subsequently used by hundreds of men. In addition, each of the four components of COMP-4 have been used individually by thousands of people around the world, again with minimal published side effects. The main goal of this study is to evaluate whether COMP-4, based on its ability to stimulate NO production by the endothelial cells, can improve FMD and attenuate serum IL-8 and PAI-1 levels in humans. 35 participants comprising men and women between the ages 18 to 39 years of age will be recruited. The investigators will then contact the participants that showed interest in the study by either a phone call or a video call, depending on participants' preferences, and the investigators will go over the consent form with the subjects. The investigators will ask participants to avoid eating any food for 6 hours and consuming nicotine and caffeine for at least 4 hours prior to both pre- and post-supplementation appointments. There is evidence that fatty meals, glucose loading, nicotine, and caffeine can impair flow mediated dilation (FMD) postprandially. Furthermore, The investigators will also ask participants, who are taking other medications, to take their medications at the same time on the morning of both of their pre- and post-supplementation appointments. The investigators will also attempt to schedule both meetings at the same time for each participant. At the initial in-person meeting with the participants, the investigators will draw blood to measure baseline serum PAI-1 and IL-8 concentrations. Baseline FMD of the brachial artery will be performed. Patients will then rest in a seated position at a 25°C room for approximately 5-10 minutes prior to measuring the heart rate and blood pressure. Using a 20 megahertz ultrasound, the brachial artery of the dominant hand will be identified immediately above the wrist at a location with no branching points and clear anterior and posterior walls. Patient's hand will be immobilized on a hand cast, and the ultrasound probe will be locked in place with knob holders. Baseline diameter of the brachial artery is measured, and blood pressure cuff will be inflated by 50 mmHg higher than patient's systolic blood pressure for a duration of 5 minutes. Diameter of the brachial artery will be measured at 30, 60, and 90 seconds immediately after deflating the cuff, and the largest diameter will be used to measure the FMD percentage compared to baseline. At the appointment's closure, participants will receive a bottle containing 60 capsules of COMP-4 (consisted of 125 mg each of ginger root, muira puama and Paullinia cupana as well as 400 mg of L-citrulline), and the participants will be instructed to take 2 capsules twice a day for a total of 14 days. At this time, each participant will also receive a Side Effect Tracker log to complete throughout the study. Participants will then be instructed to return for a second appointment at day 14 of starting COMP-4 supplementation. Serum IL-8, serum PAI-1, and FMD of the brachial artery will be measured similar to their initial visit. The investigators will ask participants to bring supplement bottles to the final visit to assess for study compliance by counting the number of pills left in the provided bottle. To monitor for safety, participants will be called twice (at day 3 and 7 after starting their COMP-4 supplement) to confirm that the subjects have been taking the supplement as instructed without bothersome side effects. In presence of bothersome side effects, participants will be withdrawn from the study. Data and Safety Monitoring Plan can be found in the attached study protocol file. The data from pre- and post-supplementation with COMP-4 will be compared using a paired-sample t-test. Statistical significance will be defined as P < .05.


Recruitment information / eligibility

Status Recruiting
Enrollment 35
Est. completion date November 30, 2023
Est. primary completion date September 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 39 Years
Eligibility Inclusion Criteria: - All men and women ages 18-39 will be offered the opportunity to participate in this study as long as they do not have a history of acute or chronic cardiovascular illnesses effecting flow mediated dilation. Exclusion Criteria: - Men and women with ages other than of 18-39 years of age; - Women who are currently pregnant; - Men and women with a history of serious cardiovascular events, those currently on blood pressure medications, and those with known allergies to any of the 4 components of COMP-4 (ginger, muira puama,Paullinia cupana, and L-citrulline)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
COMP-4
COMP-4 is a novel compound that consists of ginger extract, L-citrulline, and the herbal components Paullinia cupana and muira puama.

Locations

Country Name City State
United States UCLA Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
University of California, Los Angeles

Country where clinical trial is conducted

United States, 

References & Publications (4)

Haptonstall KP, Choroomi Y, Moheimani R, Nguyen K, Tran E, Lakhani K, Ruedisueli I, Gornbein J, Middlekauff HR. Differential effects of tobacco cigarettes and electronic cigarettes on endothelial function in healthy young people. Am J Physiol Heart Circ Physiol. 2020 Sep 1;319(3):H547-H556. doi: 10.1152/ajpheart.00307.2020. Epub 2020 Jul 31. — View Citation

Nguyen S, Rajfer J, Shaheen M. Safety and efficacy of daily Revactin(R) in men with erectile dysfunction: a 3-month pilot study. Transl Androl Urol. 2018 Apr;7(2):266-273. doi: 10.21037/tau.2018.03.22. — View Citation

Papamichael CM, Aznaouridis KA, Karatzis EN, Karatzi KN, Stamatelopoulos KS, Vamvakou G, Lekakis JP, Mavrikakis ME. Effect of coffee on endothelial function in healthy subjects: the role of caffeine. Clin Sci (Lond). 2005 Jul;109(1):55-60. doi: 10.1042/CS20040358. — View Citation

Whisner CM, Angadi SS, Weltman NY, Weltman A, Rodriguez J, Patrie JT, Gaesser GA. Effects of Low-Fat and High-Fat Meals, with and without Dietary Fiber, on Postprandial Endothelial Function, Triglyceridemia, and Glycemia in Adolescents. Nutrients. 2019 Nov 2;11(11):2626. doi: 10.3390/nu11112626. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary To study the effect of short-term use of daily COMP-4 on flow mediated dilation (FMD) of the brachial artery in young, generally healthy men and women. Flow Mediated Dilation (FMD) is a non-invasive procedure in which the response of the blood vessel to ischemia is measured. This procedure is mediated primarily by nitric oxide (NO). COMP-4 is a supplement that has been shown to increase NO availability. The investigators want to study whether COMP-4 will FMD compared to baseline. 35 subjects in approx. 9 months
Primary To investigate whether, through reduction in oxidative stress, COMP-4 can lower PAI-1 and IL-8 levels PAI-1 and IL-8 are two serum markers that are highly associated with cellular senescence, referring to permanent exit of cells from the cell cycle. Cellular senescence is associated with advancing age, and nitric oxide (NO) is one of the mechanisms shown to cause senescence. In this study, the investigators want to evaluate whether COMP-4, a supplement shown to improve NO availability, can alleviate senescence by decreasing serum markers associated with it. 35 subjects within approx. 9 months.]
Secondary To further evaluate for side effects of COMP-4 use COMP-4 consists of 4 natural compounds of ginger root, muira puama and Paullinia cupana as well as 400 mg of L-citrulline. A 3-month long pilot study by Nguyen looked at the safety profile of COMP-4 twice daily and found it to have a high safety profile. This is not surprising given all four components of COMP-4 have been shown to be safe and are naturally occurring. Given our study is the first trial in our knowledge to investigate the effect of COMP-4 on several parameters in humans, the investigators will continue to assess for side effect profile of this supplement. 35 subjects will take COMP-4 for 14 days
See also
  Status Clinical Trial Phase
Completed NCT05433233 - Effects of Lifestyle Walking on Blood Pressure in Older Adults With Hypertension N/A
Recruiting NCT06032065 - Sequential Multiple Assessment Randomized Trial of Exercise for PAD: SMART Exercise for PAD (SMART PAD) Phase 3
Completed NCT05293730 - Trial of the Impact of the Electronic Frailty Integrated With Social Needs N/A
Recruiting NCT03932162 - Gene Expression Changes In Young and Geriatric Skin Early Phase 1
Completed NCT04064528 - Effects of Age on Amino Acid Delivery to Tendon N/A
Completed NCT03366129 - Blood-Brain Barrier Disruption in People With White Matter Hyperintensities Who Have Had a Stroke
Completed NCT06029920 - Influence of Overground Walking on Biomarkers, Cognitive Function, and Quality of Life in Elderly With Mild Cognitive Impairment N/A
Recruiting NCT05566938 - Study to Design a Precision Nutrition Strategy at a Group Level in the Elderly N/A
Recruiting NCT05543980 - Leg Heat Therapy in Elderly Individuals Phase 2
Completed NCT04894929 - Comprehensive Geriatric Assessment in the Monitoring of Functional Improvement N/A
Not yet recruiting NCT06071130 - Emotion, Aging, and Decision Making N/A
Enrolling by invitation NCT04641663 - Multi-target Dietary Supplement Tolerability in an Aging Population (MTDSST) N/A
Completed NCT04088006 - The Evaluation of Efficacy and Safety of Hyaluronic Acid Injection on Skin Moisturization and Elasticity N/A
Completed NCT03695081 - Patient Pathway Pharmacist - Optimal Drug-related Care N/A
Recruiting NCT05424263 - Acetate and Age-associated Arterial Dysfunction Phase 2
Completed NCT05601713 - Mitigating Heat-induced Physiological Strain and Discomfort in Older Adults Via Lower Limb Immersion and Neck Cooling N/A
Completed NCT04551339 - Zinc Versus Multivitamin Micronutrient Supplementation in the Setting of COVID-19 N/A
Recruiting NCT04997577 - Speech Perception and High Cognitive Demand N/A
Completed NCT05922475 - Efficacy of Pre-sleep or Post-exercise Protein During 12 Weeks of Resistance Exercise Training N/A
Completed NCT04015479 - Peanut Protein Supplementation to Augment Muscle Growth and Improve Markers of Muscle Quality and Health in Older Adults N/A