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Nicotinamide Mononucleotide in Hypertensive Patients

Pilot Study of Nicotinamide Mononucleotide Supplementation in Patients With Hypertension

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04903210
Enrollment
20
Registered
2021-05-26
Start date
2021-06-01
Completion date
2022-07-31
Last updated
2022-02-01

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

Conditions

Hypertension

Keywords

Hypertension, β-nicotinamide mononucleotide, Vascular function, Blood pressure

Brief summary

Cardiovascular and cerebrovascular diseases are most terrible killers endangering the health of Chinese residents, and hypertension is the most important risk factor. Hypertension related vascular function and structural damage are the common pathological basis and initiation of cardiovascular and cerebrovascular disease. Therefore, reducing blood pressure and delaying or reversing vascular injury is an effective way to treat hypertension and prevent cardiovascular disease. NAD+ (nicotinamide adenine dinucleotide) is a coenzyme of many kinds of dehydrogenases in the body, and is an essential molecule in the basic process of life support. The latest research found that with the growth of age, the level of NAD+ is decreasing, and increasing the content of NAD+ can prolong the life of multiple species including human. NMN (β - nicotinamide mononucleotide) is a natural NAD+ precursor in cells. Recent clinical trials found that NMN supplementation can effectively improve the level of NAD+ in cells, delay aging, improve the metabolic process of cells without adverse reactions. However, the effect of NMN supplementation on reducing blood pressure and protecting vascular endothelial function has not been reported. Therefore, this study aims to focus on hypertension, a major chronic disease, and to observe the effects of NMN supplementation on vascular function and blood pressure in patients with hypertension, so as to provide a new treatment strategy for hypertension and associated vascular injury.

Interventions

DIETARY_SUPPLEMENTNicotinamide mononucleotide supplied as 400mg capsule

NMN10000 WRIGHT LIFE® + lifestyle modification NMN10000 WRIGHT LIFE®: 800mg, qd, for two months. Lifestyle modification: intake 1400-1600 kcal/day: 54% carbohydrates, 24% proteins, 22% lipids, 108 mg cholesterol, 35 g fiber; avoid smoking and alcohol consumption; performing aerobic activity 4 days per week such as 45 min on a stationary bicycle.

BEHAVIORALLifestyle modification

Lifestyle modification: intake 1400-1600 kcal/day: 54% carbohydrates, 24% proteins, 22% lipids, 108 mg cholesterol, 35 g fiber; avoid smoking and alcohol consumption; performing aerobic activity 4 days per week such as 45 min on a stationary bicycle.

Sponsors

First Affiliated Hospital, Sun Yat-Sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Study biostatistician will be blinded to group (NMN vs. controls)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Mild essential hypertensive patients (BP ranged from 130/80 to 159/99 mmHg). * Ability to undergo Study procedures. * Willingness/ability to provide informed consent.

Exclusion criteria

* Participants with secondary hypertension. * Participants suffering from diabetes mellitus, coronary heart disease, peripheral vascular disease, acute or chronic liver disease, renal insufficiency, malignancies, infectious disease, or using non-steroidal anti-inflammatory drugs, steriods, vasoactive agents. * Known allergies to niacin or nicotinamide. * Receiving certain concurrent supplements. * Women who are currently pregnant or who wish to become pregnant over the course of the study follow-up or who are at suckling period. * Unwillingness/inability to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Effect of NMN on flow mediated dilation (FMD)Up to 2 monthChange of FMD between NMN-treated participants and non-NMN-treated participants
Effect of NMN on brachial-ankle pulse wave velocity (baPWV)Up to 2 monthChange of baPWV between NMN-treated participants and non-NMN-treated participants

Secondary

MeasureTime frameDescription
Effect of NMN on blood pressureUp to 2 monthChange of systolic blood pressure and diastolic blood pressure between NMN-treated participants and non-NMN-treated participants
Effect of NMN on PBMC NAD+ levelsUp to 2 monthChange of peripheral blood mononuclear cells NAD+ levels between NMN-treated participants and non-NMN-treated participants
Effect of NMN on sleep qualityUp to 2 monthChange of the scores of Pittsburgh Sleep Quality Index (PSQI). The final score ranges from 0 to 21. The higher the score, the worse the sleep quality.
Incidence of Treatment Adverse EventsUp to 2 monthAdverse Events

Countries

China

Contacts

Primary ContactJun Tao
taojungz123@163.com+86 13922191609
Backup ContactYumin Qiu
qiuym8@mail2.sysu.edu.cn+86 18022232920

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026