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Recruiting Phase 2 NCT06629324

Evaluating Bone Marrow Cell Transplant for Treating Cerebral Palsy From Brain Hypoxia

Trial Parameters

Condition Autism Spectrum Disorder
Sponsor Vinmec Research Institute of Stem Cell and Gene Technology
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 58
Sex ALL
Min Age 1 Year
Max Age 10 Years
Start Date 2024-10-15
Completion 2026-10-15
Interventions
Autologous Bone Marrow Mononuclear Cell TransfusionRehabilitation

Brief Summary

This clinical trial aims to evaluate the effectiveness of autologous bone marrow mononuclear cell transfusion in treating cerebral palsy caused by cerebral hypoxia. The key questions the study seeks to answer are: * What is the safety profile in terms of adverse events (AE) and serious adverse events (SAE) observed over the 9 months following the first transplantation? * How does autologous bone marrow mononuclear cell (BM MNC) transplantation impact the gross motor function (GMFM-88) scores and Gross Motor Function Classification System (GMFCS) scores in children with cerebral palsy? * How does autologous BM MNC transplantation influence muscle tone (Modified Ashworth Scale score) and hand motor function (MACS/Mini-MACS scale) in children with cerebral palsy, 9 months post the initial transplantation? Fifty-eight selected patients, aged 1 to 10 years and diagnosed with spastic cerebral palsy due to brain hypoxia, will be randomly divided into two groups: * Group A: will receive two BM MNC infusions with the first at baseline and the second at 6 months ± 21 days (T6) via the spinal route. * Group B: will serve as the control group for the first 9 months. During this period, patients will not receive cell transplantation but will undergo a similar rehabilitation and medication regimen as Group A. After 9 months, Group B will receive two BM MNC infusions: the first at 9 months ± 21 days (T9) and the second at 15 months ± 21 days (T15) via the spinal route, with a follow-up at 18 months ± 21 days (T18) compared to baseline. * Both groups: will undergo rehabilitation for 10 days per month, three times, either at rehabilitation centers or performed by a rehabilitation technician at home. After this period, continued training will be conducted by family members. The combined medication regimen will include muscle relaxants (if muscle spasticity is present), vitamins, and neuroprotective drugs (Piracetam).

Eligibility Criteria

Inclusion Criteria: * Age from 1 to 10 years, both genders; * Gross Motor Function Classification System (GMFCS): levels II to V; * Spastic cerebral palsy due to brain hypoxia. Exclusion Criteria: * Coagulation disorders; * Severe health conditions such as cachexia, heart failure, lung, liver, or kidney failure; or active infections; * Spinal injuries prevent the placement of a catheter through the spinal cavity; * Cancer; * HIV positive, active viral hepatitis; * Hemoglobin below 110 g/L.

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