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Safety and Efficacy of Stem Cell Therapy in Patients With Autism

Phase Ι/Π Study of Stem Cell Therapy in Patients With Autism

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01343511
Enrollment
37
Registered
2011-04-28
Start date
2009-03-31
Completion date
2011-05-31
Last updated
2011-10-14

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

Conditions

Autism

Keywords

Autism, human cord blood mononuclear cells, human umbilical cord mesenchymal stem cells

Brief summary

Autism is one of those disorders in Autism spectrum disorders (ASD), which characterized by social interaction abnormalities, impaired verbal and non-verbal communication, and repetitive, obsessive behavior, while the therapeutic effect of current treatments remains limited progress .Neural hypoperfusion and immune deregulation are the two key pathologies associated with Autism. Human umbilical cord mesenchymal stem cells (hUC-MSCs) and human cord blood mononuclear cells (hCB-MNCs) have been shown to have the ability to modulate the immune response and enhance angiogenesis, suggesting the novel and promising therapeutic strategy. In this study, the safety and efficacy of hUC-MSCs and hCB-MNCs transplantation will be evaluated in patients with Autism.

Detailed description

To investigate the safety and efficacy of human cord blood mononuclear cells and human umbilical cord mesenchymal stem cells transplantation in patients of Autism.

Interventions

Participants will be given rehabilitation therapy plus hCB-MNCs transplantation.

Participants will be given rehabilitation therapy plus and hCB-MNCs and hUC-MSCs transplantation.

Sponsors

Shandong Jiaotong Hospital
CollaboratorUNKNOWN
Association for the Handicapped Of Jinan
CollaboratorUNKNOWN
Shenzhen Beike Bio-Technology Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Children between the ages of 3 and 12 years. * DSM-IV diagnosis of Autistic Disorder. * Total score of CARS ≥ 30. * Parents or legal guardian willing to sign the ICF.

Exclusion criteria

* Any history of hypersensitivity to serum products, or other known drug and food allergy. * History of prior or current DSM-IV psychotic disorder (e.g., schizophrenia, bipolar disorder, other psychosis), Pervasive Developmental Disorder not otherwise specified (PDD NOS), Asperger's, or Rett's. * History of Epileptic seizure activity in the past 6 months. * Autism caused by seizure disorders (active), cerebrovascular disease or brain trauma. * The global autism ratings are assessed as being absent, minimal or mild. * Existing moderate or severe extrapyramidal symptoms (EPS) or history of tardive dyskinesia. * Subjects who have displayed significant self-injurious behavior (children who have caused visible harm to themselves). * HIV+ * Acute and chronic hepatitis. * Autoimmune disease, e.g. lupus erythematosus, multiple sclerosis. * Severe pulmonary and hematological disease, malignancy or hypo-immunity. * Currently undertaking other treatment that may affect the safety/efficacy of stem cells. * Enrollment in other trials in the last 3 months. * Other criteria the investigator consider improper for inclusion.

Design outcomes

Primary

MeasureTime frame
Childhood Autism Rating Scale,CARS6 months after treatment
Clinical Global Impression Scale,CGI6 months after treatment

Secondary

MeasureTime frame
Aberrant Behavior Checklist,ABC6 months after treatment
Adverse Event and Serious Adverse Event6 months after treatment

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026