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Clinical Trials/NCT02879110
NCT02879110
Completed
N/A

A 12-weeks, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Related Mechanism of Sulforaphane in Treatment of Autism Spectrum Disorder

Central South University2 sites in 1 country110 target enrollmentAugust 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Autism Spectrum Disorder
Sponsor
Central South University
Enrollment
110
Locations
2
Primary Endpoint
The change of social impairments of children with autism spectrum disorder
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

In this proposed study, the investigators will evaluate the the efficacy, safety and related mechanism of sulforaphane in treatment of autism spectrum disorder (ASD). The study will recruit 120 ASD patients, then these patients will be randomized to sulforaphane group or placebo group (60 patients per arm) for 12 weeks clinic trial. Clinical efficacy and safety assessment will be done at screen/baseline, 4 week, 8 week and 12 week. The specific aims are to compare sulforaphane versus placebo on: 1) clinical core symptoms; 2) other behavioral problems and adaptive behaviors. Biological samples also will be collected, and stored to research related mechanisms.

Detailed Description

In this proposed study, the investigators will evaluate the the efficacy, safety and related mechanism of sulforaphane in treatment of autism spectrum disorder (ASD). The study will recruit 120 ASD patients, then these patients will be randomized to sulforaphane group or placebo group (60 patients per arm) for 12 weeks clinic trial. Clinical efficacy and safety assessment will be done at screen/baseline, 4 week, 8 week and 12 week. The specific aims are to compare sulforaphane versus placebo on: 1) clinical core symptoms; 2) other behavioral problems and adaptive behaviors. The investigators hypothesize that (1) sulforaphane is superior to placebo in the treatment of clinical symptoms in patients with ASD, measured by the Social Responsiveness Scale, Aberrant Behavior Checklist, Repetitive Behavior Scale - Revised and Ohio State University Autism Clinical Global Impression; (2) sulforaphane is superior to placebo in the treatment of other behavioral problems and adaptive behaviors patients with ASD, measured by Achenbach's Child Behavior Checklist and Adaptive Behavior Assessment System, Second Edition; and (3) Biological samples will be collected, and stored so that the hypothesis sulforaphane may alter oxidative stress indexes or inflammatory biomarkers, and influence histone deacetylase inhibitor mechanism or inflammatory mechanism et al that may be significantly correlated with clinical improvement.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
July 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Central South University
Responsible Party
Principal Investigator
Principal Investigator

Jian-Jun Ou

Assistant researcher

Central South University

Eligibility Criteria

Inclusion Criteria

  • Aged 3 to 15 years.
  • Meet DSM-V diagnostic criteria for autism spectrum disorder, and been checked with Autism Diagnostic Interview-Revised (ADI-R) and Autism Diagnostic Observation Schedule (ADOS).

Exclusion Criteria

  • With severe physical disease (i.e. congenital heart disease, thyroid disease, diseases with severe abnormality of liver or kidney function, diseases with abnormality vision or hearing et al.)
  • With severe central nervous system disease (i.e. epilepsy et al).
  • With other specific genetic syndromes (i.e. Fragile-X syndrome, Down's syndrome et al.)

Outcomes

Primary Outcomes

The change of social impairments of children with autism spectrum disorder

Time Frame: At baseline, 4 week, 8 week and 12 week/endpoint

Social impairments are measured by Social Responsiveness Scale

Secondary Outcomes

  • The change of other behavioral problems of children with autism spectrum(At baseline, 4 week, 8 week and 12 week/endpoint)
  • The change of height as measured by Height measurement tools(At baseline and 12 week/endpoint)
  • The change of blood lipid as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of clinical symptoms of children with autism spectrum(At baseline, 4 week, 8 week and 12 week/endpoint)
  • The change of HBV test as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of urine routine test as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of rigid interests and behaviors of children with autism spectrum disorder(At baseline, 4 week, 8 week and 12 week/endpoint)
  • The change of clinical general impression of children with autism spectrum(At baseline, 4 week, 8 week and 12 week/endpoint)
  • The change of blood routine test as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of fasting blood-glucose as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of kidney function as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of heart rate as measured by stopwatch(At baseline and 12 week/endpoint)
  • The change of liver function as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of adaptive behaviors of children with autism spectrum(At baseline, 4 week, 8 week and 12 week/endpoint)
  • The change of weight as measured by weighing-machine(At baseline and 12 week/endpoint)
  • The change of thyroid function as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • The change of helicobacter pylori test as tested by clinical laboratory(At baseline and 12 week/endpoint)
  • Number of participants with treatment-related adverse events as assessed by Systematic Assessment for Treatment Emergent Effects(At 4 week, 8 week and 12 week/endpoint)

Study Sites (2)

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