Social Anxiety Disorder Study Of Paroxetine

NCT00318669 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 390

Last updated 2013-04-15

No results posted yet for this study

Summary

This study is designed to evaluate the efficacy and safety in Social Anxiety Disorder (SAD).

Conditions

  • Social Phobia

Interventions

DRUG

Paroxetine hydrochloride hydrate

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Primary Completion
2006-11-30
Completion
2006-11-30

Countries

  • Japan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00318669 on ClinicalTrials.gov