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Umbilical Cord Blood vs Personalized Treatments for Improving Autistic Disorder

Autistic Spectrum Disorder Clinical Trial

Official title:
Comparison of Umbilical Cord Blood vs Personalized Treatment for Improving Autistic Spectrum Disorder

Clinical Trial Summary

The clinical study evaluates in an open-label, crossover design the comparative efficacy and safety of intranasal oxytocin and autologous umbilical cord blood for improving the functioning of children with autistic spectrum disorder

Clinical Trial Description

Children aged 3-7 years diagnosed with autistic spectrum disorder and who did not previously receive oxytocin or umbilical cord blood treatments, will be enrolled to receive both treatments in random order. Assessment of functioning impairment will be done with QCHAT/M-CHAT/CAST questionnaires initially, at 2 months, 6 months and 1 year after first treatments. Either oxytocin or cord blood will be administered initially and at visit 2, which will take place at 2 months. All children will receive both treatments. A total of 25-40 children are expected to enroll and complete the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04007224
Study type Interventional
Source Fundatia Bio-Forum
Contact
Status Completed
Phase Phase 1
Start date January 17, 2019
Completion date July 10, 2023
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