CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 48 enrolled
Drug / intervention
Sulforaphane +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02909959
NCT02909959Phase 2Completed

A Phase II, Randomized, Double-blind, Placebo-controlled Study of Myrosinase-enriched Glucoraphanin, a Sulforaphane Precursor System, in Autism Spectrum Disorder

University of North Carolina, Chapel Hill·interventional·Posted Sep 21, 2016·Updated Jun 4, 2020

In Brief

A Phase 2 clinical trial evaluating Sulforaphane and Placebo for Autism Spectrum Disorder and 3 related conditions. Completed, enrolled 48 participants across 1 site.

Detailed Summary

The aim of this randomized controlled trial is to determine if a nutritional supplement containing broccoli sprout and seed extracts, a rich source of sulforaphane, is effective in reducing core symptoms of autism spectrum disorder (ASD). The study will also explore the safety and tolerability of a sulforaphane supplement in young men with ASD, as well as its effects on challenging neuropsychiatric symptoms that are commonly associated with ASD, such as hyperactivity, irritability, and repetitive movements.

Study Details

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedSep 21, 2016
Enrollment StartMar 1, 2017
Primary CompletionMay 30, 2019
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 9.8 years ago

Interventions

Sulforaphanedrug

The investigational medicinal product is an uncoated tablet containing both glucoraphanin and myrosinase, the enzyme that converts glucoraphanin to sulforaphane in vivo. Participants in this arm will take 3-8 tablets by mouth once daily (dose depending upon weight) for 12 weeks.

Placebodrug

Placebo tablets are uncoated and matched in appearance to the investigational medicinal product, containing inert components. Participants in this arm will take 3-8 tablets by mouth once daily (dose depending upon weight) for 12 weeks.