Atomoxetine in Veterans With Comorbid ADHD/PTSD

PHASE4CompletedINTERVENTIONAL
Enrollment

44

Participants

Timeline

Start Date

October 15, 2014

Primary Completion Date

March 2, 2017

Study Completion Date

April 14, 2017

Conditions
Post Traumatic Stress DisorderAttention Deficit Hyperactivity Disorder
Interventions
DRUG

Atomoxetine 80 MG

Subjects will be randomized and assigned by the study investigator into crossover group 1 (Atomoxetine 80mg at Phase I, then placebo at Phase II) or group 2 (placebo at Phase I, then Atomoxetine at Phase II) with both placebo and medication administered through pharmacy. There was a 1-week interval between the two phases.

Trial Locations (1)

29401-5799

Ralph H. Johnson VA Medical Center, Charleston, SC, Charleston

All Listed Sponsors
lead

VA Office of Research and Development

FED

NCT02287038 - Atomoxetine in Veterans With Comorbid ADHD/PTSD | Biotech Hunter | Biotech Hunter