drugset / Trial / NCT02204410

Omega-3 Supplementation to ADHD Medication in Children

NCT02204410

Phase 4 Completed 21 enrolled Massachusetts General Hospital
NaSingle-groupOpen-labelTreatment

Summary

This study is a 12-week open-label trial to assess the effectiveness of Omega-3 fatty acids for deficient emotional self-regulation (DESR) as a supplement to Attention Deficit/Hyperactivity Disorder (ADHD) treatment in children and adolescents with Attention Deficit/Hyperactivity Disorder. Subjects will be between the ages of 6-17 and will currently be on medication for their Attention Deficit/Hyperactivity Disorder but still experience DESR traits.

Timeline

Start
2014-07
Primary completion
2016-05
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Lovaza Other / unclassified
Background Amphetamine Unknown
Background Dextroamphetamine Small molecule
Background Guanfacine Small molecule
Background Lisdexamfetamine Dimesylate Small molecule
Background Methylphenidate Small molecule
Background dexmethylphenidate Unknown