ClinicalTrials.gov record
Completed Phase 2 Interventional Accepts healthy volunteers Results available

Nepicastat for Posttraumatic Stress Disorder (PTSD) in OIF/OEF Veterans

ClinicalTrials.gov ID: NCT00659230

Public ClinicalTrials.gov record NCT00659230. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 4, 2026, 1:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Placebo-Controlled Trial of the Dopamine-B-Hydroxylase (DBH) Inhibitor, Nepicastat, for the Treatment of PTSD in OIF/OEF Veterans

Study identification

NCT ID
NCT00659230
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tuscaloosa Research & Education Advancement Corporation
Other
Enrollment
100 participants

Conditions and interventions

Interventions

  • Nepicastat Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
19 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2009
Primary completion
Jul 4, 2012
Completion
Aug 29, 2012
Last update posted
Oct 12, 2017

2009 – 2012

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Tuscaloosa VAMC Tuscaloosa Alabama 35404
VA San Diego Healthcare System San Diego California 92161
James J.Peters VA Medical Center The Bronx New York 10468

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00659230, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 12, 2017 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00659230 live on ClinicalTrials.gov.

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