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Clinical Research on the Evaluation of the Efficacy and Safety of Mesenchymal Stem Cell Therapy for Vascular Aging

Clinical Research on the Evaluation of the Efficacy and Safety of Mesenchymal Stem Cell Therapy for Vascular Aging

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101200
Enrollment
Unknown
Registered
2025-04-22
Start date
2025-05-15
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Vascular aging

Interventions

hUC-MSCs intervention group:Conventional drug therapy + hUC-MSCs
External control group 1- conventional treatment group:Conventional drug therapy
External control group 2- lifestyle group:Conventional medication + lifestyle intervention

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age 60-80 years old; (2) Diagnosis: 1) Stable coronary artery disease: according to the diagnostic criteria of Chinese Guidelines for the Diagnosis and Treatment of stable coronary artery disease 2018, that is, chronic stable exertional angina, ischemic cardiomyopathy and stable disease after acute coronary syndrome; 2) old myocardial infarction: patients met the diagnostic criteria of the Guidelines for the Diagnosis and Treatment of Acute ST-segment elevation myocardial infarction with at least one coronary artery stenosis > 50%; 3) PWV > 1800. (3) Be able to cooperate with the completion of the assessment and follow-up; (4) Patients voluntarily participated in the study and provided written informed consent by themselves or their legal representatives. (5) Life expectancy over 12 months; (6) Not participating in other intervention studies during the same period.

Exclusion criteria

Exclusion criteria: (1) patients with severe cardiovascular diseases (such as unstable angina pectoris, myocardial infarction, severe heart failure, etc.); (2) patients with chronic wasting diseases such as severe liver and kidney insufficiency and malignant tumors; (3) patients with diseases affecting cognition (such as dementia); (4) stroke, uncontrolled hypertension or hyperglycemia; Drug or alcohol abuse; (5) patients with autoimmune diseases; Presence of active infection, including antibodies to hepatitis B, hepatitis C, or hepatitis C HIV antibody positive); (6) planned organ transplantation; (7) frailty caused by other diseases or in the acute stage of illness; (8) have allergic constitution or positive history of drug allergy, or have been clearly allergic to stem cells or related preparations; (9) there are other conditions that may affect physical health.

Design outcomes

Primary

MeasureTime frame
Pulse Wave Velocity;

Secondary

MeasureTime frame
Intima-media thickness of carotid and peripheral arteries, IMT;Adverse cardiovascular and cerebrovascular events, MACE;Interleukin, IL;High-sensitivity C-reactive protein, Hs-CRP;Nicotinamide adenine dinucleotide, NAD+;Endothelial cell microparticles, EMPs;B-type natriuretic peptide, BNP;Homocysteine, Hcy;Lymphocyte subpopulation;Vasodilatory function, FMD;The reactive hyperemia index, RHI;Ankle-brachial index, ABI;A 6-minute walk test was performed, 6MWT;SF-36;Mental state assessment scale, HAD;Blood pressure;Abdominal girth;Body mass index, BMI;Glycosylated hemoglobin, HbA1c;

Countries

China

Contacts

Public ContactCao Feng

Chinese PLA General Hospital

fengcao8828@163.com+86 139 1179 8280

Outcome results

None listed

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