Clinical Trials Directory

Trials / Completed

CompletedNCT00205491

Pharmacological Intervention in Depression After Traumatic Brain Injury

Pharmacological Intervention in Depression After Traumatic Brain Injury (A Research Study Within the Traumatic Brain Injury Model System)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Virginia Commonwealth University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if treatment with venlafaxine reduces symptoms of depression in persons with traumatic brain injury.

Detailed description

The study evaluates the benefits of a promising antidepressant medication for the treatment of persons with traumatic brain injury (TBI) and major depressive disorder (MDD). The study is a randomized, double-blind, placebo-controlled trial of venlafaxine (a serotonin and norepinephrine reuptake inhibitor, also known as Effexor). Venlafaxine has been well established in the treatment of MDD in healthy individuals and is a recommended depression treatment agent for persons with TBI. By using a rigorous scientific methodology, this study will be an important first step in advancing the treatment of depression in this population beyond general impressions to proven treatments.

Conditions

Interventions

TypeNameDescription
DRUGVenlafaxine

Timeline

Start date
2004-10-01
Primary completion
2007-09-01
Completion
2007-09-01
First posted
2005-09-20
Last updated
2017-03-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00205491. Inclusion in this directory is not an endorsement.

Pharmacological Intervention in Depression After Traumatic Brain Injury (NCT00205491) · Clinical Trials Directory