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Efficacy comparison and safety assessment of autologous cord blood and umbilical plasma infusion on cerebral palsy

Efficacy comparison and safety assessment of autologous cord blood and umbilical plasma infusion on cerebral palsy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034756
Enrollment
Unknown
Registered
2020-07-17
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-07-20

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

Conditions

Cerebral palsy

Interventions

Autologous cord blood group:Infusion of autologous cord blood mononuclear cells
Autologous umbilical plasma group:Infusion of autologous umbilical plasma
Placebo control group:Infusion of normal saline

Sponsors

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.3 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Children who are diagnosed with cerebral palsy in our department from 3 months to 10 years old, regardless of gender; 2. Willing to follow all learning methods; 3. The umbilical cord blood group” requires that autologous cord blood be retained and willing to accept autologous cord blood infusion; 4. The "umbilical plasma group" requires willingness to inject autologous umbilical plasma; 5. The "control group" is the children who volunteered to participate in this study but refused autologous umbilical cord blood or umbilical plasma transfusion.

Exclusion criteria

Exclusion criteria: 1. There is a known genetic disease; 2. There are major organ diseases: such as severe microcephaly, refractory epilepsy, autism, progressive neurological disease, tachyarrhythmia, heart/lung/liver/kidney and other organ damage; 3. Have received cell therapy in the past, or need primary cell disease treatment; 4. There is a drug allergy related to this study; 5. The guardian's cooperation is not good, including uncoordinated rehabilitation and follow-up.

Design outcomes

Primary

MeasureTime frame
Neuropsychological development;Immune Function;Head MR examination;

Secondary

MeasureTime frame
Organ function;Genetic examination;

Countries

China

Contacts

Public ContactZhanwen He

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

hezhanw@mail.sysu.edu.cn+86 18802033743

Outcome results

None listed

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