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 Omega 3 fatty acid Other / unclassified — —
Background Adderall Unknown — —
Background Amphetamine Unknown — —
Background Dextroamphetamine Small molecule — —
Background Guanfacine Small molecule — —
Background Lisdexamfetamine Dimesylate Small molecule — —
Background Methylphenidate Small molecule — —
Background Stratterra Unknown — —
Background dexmethylphenidate Unknown — —