Project to Improve Symptoms and Mood in People With Spinal Cord Injury

PHASE4CompletedINTERVENTIONAL
Enrollment

133

Participants

Timeline

Start Date

July 31, 2007

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
Major Depressive DisorderDysthymiaSpinal Cord Injuries
Interventions
DRUG

venlafaxine XR

Once daily oral dose of venlafaxine XR ranging from 37.5 mg up to 300 mg

DRUG

placebo

Once daily oral dose of placebo ranging from 37.5 mg up to 300 mg

Trial Locations (6)

33124

University of Miami, Miami

75246

Baylor Institute for Rehabilitation, Dallas

98104

University of Washington/Harborview Medical Center, Seattle

35294-0111

University of Alabama, Birmingham

60611-2654

Rehabilitation Institute of Chicago, Chicago

48109-0491

University of Michigan, Ann Arbor

All Listed Sponsors
collaborator

University of Michigan

OTHER

collaborator

Shirley Ryan AbilityLab

OTHER

collaborator

University of Alabama at Birmingham

OTHER

collaborator

Baylor Health Care System

OTHER

collaborator

University of Miami

OTHER

collaborator

New York University

OTHER

lead

University of Washington

OTHER

NCT00592384 - Project to Improve Symptoms and Mood in People With Spinal Cord Injury | Biotech Hunter | Biotech Hunter