Autistic Disorder Clinical Trial
Official title:
Autologous Bone Marrow Stem Cell Therapy for Autism: An Open Label Uncontrolled Clinical Trial
| Verified date | December 2015 |
| Source | Vinmec International Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Vietnam: Hanoi Department of Health |
| Study type | Interventional |
The aim of this study was to evaluate the safety and effectiveness of autologous bone marrow mononuclear stem cells in the management of autism.
| Status | Completed |
| Enrollment | 24 |
| Est. completion date | December 2015 |
| Est. primary completion date | December 2015 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 3 Years to 16 Years |
| Eligibility |
Inclusion Criteria: - Confirmed diagnosis of autism according to the Diagnostic and Statistical Manual-IV (DSM-IV) diagnostic criteria for autistic disorder Exclusion Criteria: - Epilepsy - Hydrocephalus with ventricular drain - Coagulation disorders - Allergy to anesthetic agents - Severe health conditions such as cancer, failure of heart, lung, liver or kidney - Active infections - Severe psychiatric disorders |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Vietnam | Vinmec International Hospital | Hanoi |
| Lead Sponsor | Collaborator |
|---|---|
| Vinmec International Hospital |
Vietnam,
Sharma A, Gokulchandran N, Sane H, Nagrajan A, Paranjape A, Kulkarni P, Shetty A, Mishra P, Kali M, Biju H, Badhe P. Autologous bone marrow mononuclear cell therapy for autism: an open label proof of concept study. Stem Cells Int. 2013;2013:623875. doi: 10.1155/2013/623875. Epub 2013 Aug 25. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in Total Score of Childhood Autism Rating Scale (CARS) | CARS | 3 months and 6 months after transplantation | No |
| Primary | Number of adverse events | Examples of adverse events to look for: vomiting, increased hyperactivity, fever, bleeding, hematoma, seizures and neurological deficits | Through study completion, an average of 6 months | Yes |
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