Overview

Antidepressant Prophylaxis for Interferon-Induced Depression: Efficacy of Paroxetine

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
Objectives: 1. To determine whether paroxetine can prevent major depression in patients with hepatitis C (HCV) who are receiving pegylated-interferon (Peg-IFN). 2. To determine whether paroxetine can prevent subsyndromal increases in depression and anxiety in patients with HCV who are receiving Peg-IFN. 3. To determine whether paroxetine can prevent a significant change in the health related quality of life in patients with HCV who are receiving Peg-IFN. 4. To determine whether paroxetine improves compliance with Peg-IFN therapy for HCV. 5. To determine whether paroxetine enables patients to complete Peg-IFN therapy for HCV who might otherwise require a dose reduction or discontinuation because of neuropsychiatric side effects.
Phase:
Phase 4
Details
Lead Sponsor:
Portland VA Medical Center
Collaborators:
GlaxoSmithKline
Schering-Plough
Treatments:
Antidepressive Agents
Interferons
Paroxetine