Clinical Trials Directory

Trials / Completed

CompletedNCT01371435

Drug Use Investigation for PAXIL Tablet

Status
Completed
Phase
Study type
Observational
Enrollment
3,708 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
Healthy volunteers

Summary

This post-marketing surveillance study is designed to detect adverse events (particularly clinically significant adverse drug reactions) occurring in clinical settings and to examine factors likely to affect the safety and efficacy of paroxetine.

Conditions

Interventions

TypeNameDescription
DRUGParoxetine

Timeline

Start date
2001-04-01
Primary completion
2005-09-01
Completion
2005-12-01
First posted
2011-06-10
Last updated
2017-06-08

Source: ClinicalTrials.gov record NCT01371435. Inclusion in this directory is not an endorsement.