ClinicalTrials.Veeva

Menu

Evaluate the Efficacy and Safety of DHA in the Adjuvant Treatment of Children With ASD.

M

Maimónides Biomedical Research Institute of Córdoba

Status

Completed

Conditions

ASD

Treatments

Dietary Supplement: EuPoly-3 DHA Infant
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03620097
ICI14/00355

Details and patient eligibility

About

In the etiopathogenesis of autistic spectrum disorder (ASD) several hypotheses have been described that include inflammation, metabolic alterations, activation of oxidative stress, changes in the intestinal microbiota and in the elimination capacity of heavy metals. Adjuvant therapies with omega-3 polyunsaturated fatty acids could modify these alterations.

Full description

Several hypotheses have been described in the etiopathogenesis and evolution of ASD, among which is that there is greater oxidative stress associated with a proinflammatory state, or even metabolic alterations after exposure to heavy metals, as well as differences in intestinal microbiota. This situation could negatively influence the correct establishment of neuronal synapses and their functioning, which have still been poorly investigated, especially in children. In this way, an early intervention with nutritional supplements with DHA, which could be deficient in autism, could decrease the proinflammatory and oxidative stress state, favoring the formation of neuronal synapses as well as their activity. This intervention could positively influence to prevent the clinical deterioration associated with ASD and it would be of special interest in early childhood since at this stage of neurodevelopment there is maximum neuronal plasticity.

Enrollment

60 patients

Sex

All

Ages

2 to 5 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children and girls aged between 2 and 5 years diagnosed with Autism Spectrum Disorder according to the DSM-V criteria and the Observation Scale for the Diagnosis of Autism (ADOS).
  • Informed consent signed by one of the parents or legal representative.

Exclusion criteria

  • Children under 2 years old.
  • Children diagnosed with ASD over 4 years old.
  • Coexistence of another diagnosis associated with autism.
  • Patients who are receiving some type of supplement or concomitant medication that does not allow a period of washing.
  • Patients diagnosed with other pathologies or with mediation that may affect the study variables (oxidative stress, inflammation, cell adhesion molecules, lipid profile or microbiota).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups, including a placebo group

Experimental Arm
Experimental group
Description:
30 subjects will receive 800mg of DHA (Dietary Supplement: EuPoly-3 DHA Infant) per day.
Treatment:
Dietary Supplement: EuPoly-3 DHA Infant
Control Arm
Placebo Comparator group
Description:
30 children will take a placebo with similar lipid characteristics
Treatment:
Other: Placebo

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems