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Study on the Efficacy and Safety of Umbilical Cord Blood Mononuclear Cell Transplantation in Improving Aging

Study on the Efficacy and Safety of Umbilical Cord Blood Mononuclear Cell Transplantation in Improving Aging

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110704
Enrollment
Unknown
Registered
2025-10-20
Start date
2025-07-08
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Aging

Interventions

High-dose treatment group:Intravenous infusion of umbilical cord blood mononuclear cells over a period of 4 months, once per month.
High-dose treatment group:Intravenous infusion of umbilical cord blood mononuclear cells for 2 months, followed by intravenous infusion of normal saline for 2 months, with each infusion occurring once
Control Group:Equal-dose normal saline infusion

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 50 years; 2. No severe diseases in major organs; 3. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with severe diseases or unstable medical conditions caused by age-related changes in major organs; 2. History of severe allergic reactions; 3. History of malignant tumors or presence of active malignancy; 4. Active systemic or severe focal infections (including HIV and syphilis); 5. Individuals with severe psychiatric disorders or cognitive impairments; 6. Individuals with severe liver or kidney dysfunction, hematologic disorders, or diseases affecting the circulatory, respiratory, or nervous systems (moderate to severe Parkinson’s disease/Alzheimer’s disease); 7. Individuals with any immunodeficiency disease or condition; 8. Patients who, in the investigator's opinion, are unsuitable for participation in the study due to potential protocol violations or any other condition affecting their safety.

Design outcomes

Primary

MeasureTime frame
Biological age;Comprehensive Geriatric Assessment;

Secondary

MeasureTime frame
Improvement or progression of cardiovascular and cerebrovascular diseases.;Adverse reaction/event occurrence rate;IL-6;Imaging indicators;

Countries

China

Contacts

Public ContactPing Zhu

Chinese PLA General Hospital

zhuping301hospital@163.com+86 10 6829 5851

Outcome results

None listed

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