Bone Marrow-Derived Stem Cell Transplantation for the Treatment of Cerebral Palsy

NCT ID: NCT03078621

Last Updated: 2020-03-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1/PHASE2

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-09-30

Study Completion Date

2021-01-31

Brief Summary

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This study is a single arm, single center trial to study the safety and efficacy of purified autologous bone marrow derived stem cells and mesenchymal stem cells for the treatment of children with cerebral palsy.

Detailed Description

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Cerebral palsy (CP) is a chronic childhood disorder defined by a range of motor and cognitive impairments and results in a substantial suffering to the patient and a tremendous socio-economic burden to the individual, family, and healthcare system. With no effective treatments or interventions, therapies for CP are currently focused on supportive and management strategies. Stem cell transplantation has been suggested as a putative intervention for neural pathology, as mesenchymal and neural stem cells, as well as olfactory ensheathing glia and Schwann cells, which have shown some regenerative and functional efficacy in experimental central nervous system disorders.

In this trial, the investigators study the safety and efficacy of the intrathecal transplantation of specific populations of purified autologous bone marrow-derived stem cells and mesenchymal stem cells in patients with cerebral palsy.

Conditions

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Cerebral Palsy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Stem Cells

Intravenous and Intrathecal transplantation of specific populations of purified bone marrow-derived stem cells and mesenchymal stem cells.

Group Type EXPERIMENTAL

Stem Cell Therapy

Intervention Type BIOLOGICAL

Intravenous and Intrathecal transplantation of purified autologous bone marrow-derived stem cells and mesenchymal stem cells.

Interventions

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Stem Cell Therapy

Intravenous and Intrathecal transplantation of purified autologous bone marrow-derived stem cells and mesenchymal stem cells.

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Must be more than 2 year of age and less than 12 years of age at the time of screening for inclusion in the study.
* Clinical evidence of a non-progressive motor disability due to brain dysfunction.
* Willing to comply with all study procedures.
* Gross Motor Function Classification Score level II-V

Exclusion Criteria

Known history of:

* Intractable seizures
* Traumatic brain injury
* Genetic disorder
* Current Infection
* Renal insufficiency
* Hepatic disease
* HIV+ (as demonstrated by positive blood test)
* Immunosuppression
* Infectious related neurological injury
* Other etiologies such as degenerative, mitochondrial, and metabolic disorders
* Normal brain MRI
* Evidence of acute illness such as fever (temperature \> 37.5 C), vomiting, diarrhea, wheezing or crackles
* Progressing neurological disease (Batten Disease, Leukodystrophies, Neurotransmitter disorders)
* Microcephaly, macrocephaly, cortical malformations, or genetic disorders of dysgenesis
* Pulmonary disease requiring ventilator support
* Unwillingness to return for follow-up visits
* Contraindications to MRI
Minimum Eligible Age

2 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stem Cells Arabia

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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SCA-CP1

Identifier Type: -

Identifier Source: org_study_id

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