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Clinical study on the safety and efficacy of umbilical cord blood mononuclear cells in the treatment of myelopathy

Clinical study on the safety and efficacy of umbilical cord blood mononuclear cells in the treatment of myelopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099211
Enrollment
Unknown
Registered
2025-03-19
Start date
2025-03-31
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Myelopathy

Interventions

intervention group:Intrathecal injection of umbilical cord blood mononuclear cells combined with intravenous infusion

Sponsors

Shandong Provincial Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years old, gender unlimited; 2. Clinically diagnosed myelopathy; 3. No obvious abnormalities in liver and kidney function: ALT, AST<=2.5 times the normal upper limit, serum Cr and BUN<=1.25 times the normal upper limit; 4. No obvious abnormality of cardiopulmonary function; 5. Normal immune function and immune deficiency screening; 6. Sign the informed consent in accordance with the patient's personal wishes under the premise of full knowledge.

Exclusion criteria

Exclusion criteria: 1. The vital signs are unstable; 2. Combined with malignant tumors or other major systemic diseases; 3. Patients with severe active infections, or those known to be HIV-positive, or patients with hepatitis B, hepatitis C, or syphilis. 4. Serious trauma to other organs may affect subsequent safety assessment; 5. Pregnant or breastfeeding women, women of pregnant age, with the consent of their partner, must use effective contraception before and during the study and for 6 months after the study is completed. During the study period, women should notify the doctor in charge if they suspect that pregnancy is possible; 6 Allergic reaction to the drugs or similar drugs used in this study; 7 Participating in other clinical trials; 8. Patients considered unsuitable for inclusion by other investigators.

Design outcomes

Primary

MeasureTime frame
The rate at which patients achieved grade improvement on the ASIA Functional Scale;The rate at which patients achieved improvement in FIM functional scale rating;Rate of improvement in the WISCI functional scale of patients;

Secondary

MeasureTime frame
Spinal cord imaging changes of patients;

Countries

China

Contacts

Public ContactFang Long

Shandong Provincial Third Hospital

fanglong840606@126.com+86 531 81656146

Outcome results

None listed

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