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Clinical Trials/NCT04099381
NCT04099381
Recruiting
Phase 1

Protocol for Evaluating the Safety and Efficacy of Transfusion of Umbilical Cord Blood in Patients With a Diagnosis of Autism Spectrum Disorder Depending on the Degree of Tissue Compatibility of the Donor and the Recipient

State-Financed Health Facility "Samara Regional Medical Center Dinasty"1 site in 1 country150 target enrollmentAugust 10, 2019

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Autism Spectrum Disorder
Sponsor
State-Financed Health Facility "Samara Regional Medical Center Dinasty"
Enrollment
150
Locations
1
Primary Endpoint
Autism Treatment Evaluation Checklist (ATEC).
Status
Recruiting
Last Updated
3 years ago

Overview

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.

The possible reason for ASD is neural hypoperfusion and immune dysregulation. The Human Umbilical Cord Blood Mononuclear Cells (hUCB-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 hUCB-MNCs infusion will be evaluated in patients with Autism with regarding to HLA compatibility.

Detailed Description

Autism Spectrum Disorders (ASD) are heterogeneous neuro-developed disorders. Autism is the most common disorder of the diseases characterized by dysfunctions in response to social interaction and communication, as well as the presence of repetitive and stereotyped behaviors. Recent reports of a sharp increase in the number of children with autism. The exact etiology of autism remains unclear. Compliance, the definition of effective treatments for autism is particularly difficult. Although it has been understood, it can be a question of immune dysregulation. Examination of the inflammatory cytokines, dysfunction of the immune system and the immune system. The Human Umbilical Cord Blood Mononuclear Cells (hUCB-MNCs) have been shown to have the ability to modulate the immune response and enhance angiogenesis, suggesting the novel and promising therapeutic strategy. Our study suggest that infusion of cord blood mononuclear cells will affect Autism. This protocol was developed on the basis of the results of the previously approved protocol of the center NCT03786744 (Transfusion of allogeneic cord blood samples in patients with autism spectrum disorders), which showed high efficiency in the rehabilitation of patients. The present protocol is intended for revealing the dependence of the clinical effect on the degree of tissue compatibility of umbilical cord blood samples and the recipient.

Registry
clinicaltrials.gov
Start Date
August 10, 2019
End Date
May 26, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
State-Financed Health Facility "Samara Regional Medical Center Dinasty"
Responsible Party
Principal Investigator
Principal Investigator

Volchkov Stanislav

Deputy director, Quality assurance director

State-Financed Health Facility "Samara Regional Medical Center Dinasty"

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Autism Treatment Evaluation Checklist (ATEC).

Time Frame: baseline, change from baseline every month (total 12 evaluations)

Will be assessed: I. Speech/Language Communication (14 items); II. Sociability (20 items); III. Sensory/ Cognitive Awareness (18 items); and IV. Health/Physical/Behavior (25 items).

Number of participants with non-serious and serious adverse events.

Time Frame: baseline, change from baseline at 12 month

Safety assessment. Adverse events rate will be assessed in all patients.

The Childhood Autism Rating Scale (CARS2).

Time Frame: baseline, change from baseline at 6,12 month

Rating for behavior, characteristics, and abilities against the expected developmental growth. Will be assessed fifteen items, including: relationship to people; imitation; emotional response; body; object use; adaptation to change; visual response; listening response; taste-smell-touch response and use; fear and nervousness; verbal communication; non-verbal communication; activity level; level and consistency of intellectual response; general impressions. Total score will be assessed. Scores range form 15 to 60 with 30 being the cutoff rate for a diagnosis of mild autism. Scores 30-37 indicate mild to moderate autism, while scores between 38 and 60 are characterized as severe autism.

Secondary Outcomes

  • Evaluation of the survival of donor cells in the host body without immune responses(baseline, change from baseline at 6 month)
  • The correlation of the concentration of T-regulatory cells (CD4/CD25/FoxP3) in the sample of umbilical cord blood and the treatment effectiveness degree(At 1, at 6 months (At first and second infusion))
  • The correlation of the concentration of T-regulatory cells (CD4/CD25/FoxP3) in the patient depending on the severity of the disease.(At 1, at 6 months (At first and second infusion))
  • The correlation of the concentration of CD34+ cells in the cord blood sample and the treatment effectiveness degree(At 1, at 6 months (At first and second infusion))

Study Sites (1)

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