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Evaluation of Beta NMN pills in slowing the aging process in patients with heart disease

Evaluation of Epigenetic aging and its modulation by Beta-Nicotinamide Mononucleotide [Beta-NMN] in patients diagnosed with Coronary Artery Disease - NILL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/073020
Enrollment
80
Registered
2024-08-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: Beta Nicotinamide Mononucleotide: Tablet beta NMN 500 mg once a day orally for 180 days Control Intervention1: Lactose: Tablet Lactose 500mg once a day orally for 180 days

Sponsors

Indian Council of Medical Research (ICMR)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients with suspected Coronary artery disease with stable typical or atypical symptoms suspicious for coronary artery disease like chest pain chest tightness chest burning shoulder pain palpitations jaw pain or non chest pain symptoms such as dyspnea or worsening effort tolerance and who are considered to be at very low to high risk of coronary artery disease based on initial clinical assessment Willing to take beta NMN 500 mg per day for six months Willing to have blood drawn three times at baseline three months and six months

Exclusion criteria

Exclusion criteria: Patients being evaluated for other Cardiac diseases like valvular disease etiology of cardiomyopathy Patients with unstable angina who have elevated serum cardiac biomarkers ECG changes etc Patients with NSTE ACS NSTEMI and STEMI Patients with liver disease renal disease joint pain hypothyroid or hyperthyroid disease cerebrovascular disease anemia and chronic obstructive lung disease Individuals unwilling to undergo investigations or provide consent

Design outcomes

Primary

MeasureTime frame
Improvement in the quality of life DNA Methylation and NAD concentrationTimepoint: Day 0 Day 90 Day 180

Secondary

MeasureTime frame
Improvement in the six minute walking test and relative leukocyte telomere lengthTimepoint: Day 0 Day 90 Day 180

Countries

India

Contacts

Public ContactDr Melvin George

SRM Medical College Hospital and Research Centre, SRM UNIVERSITY

melving@srmist.edu.in9894133697

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026