Special Drug Use Investigation for PAXIL Tablet (20mg-Clinical Symptom Progression)

NCT01371461 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 390

Last updated 2017-06-08

No results posted yet for this study

Summary

Overall improvement, severities and changes of specific clinical symptoms were surveyed in outpatients with depression or in a depressed state to evaluate the efficacy and safety of PAXIL tablets in patients in whom the PAXIL dose was increased and those treated with a constant dose.

Conditions

  • Mental Disorders

Interventions

DRUG

Paroxetine

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-01-31
Primary Completion
2004-07-31
Completion
2004-10-31

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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 NCT01371461 on ClinicalTrials.gov