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A study to evaluate the efficacy of Coenzyme I for Injection in the treatment of vascular aging

A randomized, double-blind, parallel-controlled clinical trial to evaluate the efficacy of Coenzyme I for Injection in the treatment of vascular aging

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116222
Enrollment
Unknown
Registered
2026-01-07
Start date
2026-01-07
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Arteriosklerose

Interventions

control group:normal saline
Treatment Group:the administration of Coenzyme I for Injection

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 40 and 70 years; 2.Abnormally elevated cf-PWV, exceeding the upper limit of the reference range matched for age and blood pressure; 3.Diagnosis of Grade 1 hypertension, with systolic blood pressure between 140 and 159 mmHg and/or diastolic blood pressure between 90 and 99 mmHg; 4.Willingness to participate and provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Consumption of foods or medications containing high levels of NAD+, NR, NAM, NMN, or niacin-related components (including vitamin B3 and natural health products) within 3 months prior to screening; 2.History of major cardiovascular or cerebrovascular events, including myocardial infarction, angina pectoris, stroke, or hospitalization for arterial revascularization; 3.Systolic blood pressure =160 mmHg and/or diastolic blood pressure =100 mmHg; 4.Diagnosis of malignant tumor; 5.Known allergy or severe adverse reactions to Coenzyme I for Injection or any of its components; 6.History of severe allergies or infusion reactions; 7.Pregnancy, lactation, or women planning pregnancy; 8.Severe hepatic or renal dysfunction: ALT or AST >5 times the upper limit of normal, or glomerular filtration rate =30 mL/min/1.73 m²; 9.Concurrent participation in another clinical trial without having completed the follow-up period; 10.Other conditions deemed by the investigator as unsuitable for inclusion in this study, such as psychiatric or psychological disorders.

Design outcomes

Primary

MeasureTime frame
the change of endothelial function;

Secondary

MeasureTime frame
the change of degree of arterial stiffness;

Countries

China

Contacts

Public ContactYi Zhang

Shanghai Tenth People's Hospital

yizshcn@gmail.com+86 21 66301090

Outcome results

None listed

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