Evaluation and Treatment of Copper/Zinc Imbalance in Children With Autism
Stopped early · Phase 1 · Has a placebo group
Conditions studied: Autism, Pervasive Developmental Disorder
In brief
There are two phases to the study. The first will examine serum copper and zinc levels and copper/zinc ratio in children (ages 3-8) who have autism and compare them to levels from same sex and age children who are developing typically. The hypothesis is that there is a significant difference in the copper/zinc ratio between young children who have autism and their typically developing peers. The second phase of the study will evaluate the effect of dietary supplementation using zinc and vitamin C for 16 weeks on selected symptoms of autism. Children with autism will be enrolled on the basis of copper/zinc ratios greater than 2.0, and as determined to be statistically higher than typically developing children. Measurements of serum copper, zinc and unbound copper will be obtained prior to, at the mid-point and end of the trial. Those children whose ratios have not fallen below 1.25, the top of the currently recognized range will have the zinc and vitamin C doses adjusted for the duration of the trial. Detailed evaluation of language skills, and a variety of behaviors will be evaluated prior to and after supplementation. The study will be placebo-controlled and double blind. Those children enrolled in the placebo arm will be offered a full trial of supplements at the end of the their participation in the study. The hypothesis to be tested is whether correction of elevated copper to zinc ratios in children with autism can be accomplished by oral supplementation with zinc and vitamin C and if these children show measurable and significant changes in receptive or expressive language or behavioral parameters associated with autism.
Key facts
- Study ID
- NCT00325572
- Run by
- Milton S. Hershey Medical Center
- People needed
- 89
- Starts
- 2006-11-01
- Expected to finish
- 2011-12-01
- Last updated by the study team
- 2019-07-17
Who can join
Age: 3 and older, up to 8. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Ages 3-8 years
- Diagnosis of autism spectrum disorder
- Serum copper/zinc ratio greater than 2.0 or as determined in phase 1 of the study
You may not qualify if…
- Known chromosomal disorder or neurological disorders other than autism
Where it is running
- Penn State Children's Hospital — Hershey, Pennsylvania, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.