← Eichor
Study identifier: NCT06573970 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Atomoxetine and Executive Function in PTSD

Condition: Posttraumatic Stress Disorder With Attention Defic  ·  Sponsor: VA Office of Research and Development

PhasePhase 4
Planned participants160
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

Attention deficits (AD) frequently co-occur with posttraumatic stress disorder (PTSD). The presence of AD is associated with greater PTSD clinical severity and poorer clinical outcomes. Knowledge regarding the mechanism underlying this association is limited, though the emerging evidence has indicated that executive function deficit (EFD) is strongly correlated with AD and PTSD symptoms. While treatments developed for PTSD have existed for years, a substantial portion of individuals do not fully respond to conventional treatment. Accumulating evidence suggest that attention deficit (AD) and EFD may be a driving force for PTSD treatment resistance. However, treatment of executive impairment in PTSD is very limited. As a result, untreated co-occurring AD and EFD in PTSD poses severe negative impacts on patients' functional recovery, treatment outcomes, and quality of life (QoL). Given that up to 50% of patients do not respond well to the first-line pharmacological PTSD treatments, it is imperative to seek novel treatment strategies to improve EF that may improve both standard treatment response and QoL, social function. The proposed study directly addresses this knowledge gap by testing the efficacy of atomoxetine (ATX) in improving EF and attention among Veterans with PTSD, which will further improve Veterans' QoL and social function. ATX represents a promising novel candidate pharmacotherapy for individuals with PTSD. ATX is a non-stimulant selective norepinephrine reuptake i…

This description comes directly from the study's public registry record.

Talk to the study team

Zhewu Wang, MD  ·  (843) 789-7949  ·  zhewu.wang@va.gov

Mark B Hamner, MD BS  ·  (843) 789-7799  ·  Mark.Hamner@va.gov

Always discuss trial participation with your own doctor first.

Locations (1)

Ralph H. Johnson VA Medical Center, Charleston, SCCharleston, South Carolina, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06573970