Viewing Study NCT00196664



Ignite Creation Date: 2024-05-05 @ 11:58 AM
Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00196664
Status: COMPLETED
Last Update Posted: 2009-05-13
First Post: 2005-09-13

Brief Title: Efficacy of Paroxetine in the Prevention of Depressive Syndrome in Patients With Chronic Hepatitis C Treated by PEG-Interferon Alfa Plus Ribavirin
Sponsor: French National Agency for Research on AIDS and Viral Hepatitis
Organization: French National Agency for Research on AIDS and Viral Hepatitis

Study Overview

Official Title: Assessment of the Efficacy of Paroxetine in the Prevention of Depressive Syndrome in Patients With Chronic Hepatitis C Treated by PEG-Interferon Alfa Plus Ribavirin Multicentric Double-Blinded Randomized Study ANRS HC18 Paropeg
Status: COMPLETED
Status Verified Date: 2009-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Depression is a common side effect of interferon in the treatment of chronic hepatitis C The aim of this study is to assess the efficacy and safety of paroxetine an antidepressant agent in the prevention of depression induced by PEG-interferon given for the treatment of chronic hepatitis C
Detailed Description: The aim of this study is to assess the efficacy and safety of paroxetine an antidepressant agent in the prevention of depression induced by PEG-interferon given for the treatment of chronic hepatitis C This is a comparative study including two groups of patients randomly allocated one with paroxetine and the other with the placebo The rate of depression will be compared between the 2 groups

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
ANRS HC18 PAROPEG None None None