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Clinical Trials/NCT00182533
NCT00182533
Terminated
Phase 4

Sertraline in the Treatment of Generalized Social Phobia With Comorbidity

Hamilton Health Sciences Corporation1 site in 1 country170 target enrollmentJuly 2002

Overview

Phase
Phase 4
Intervention
Sertraline
Conditions
Phobia, Social
Sponsor
Hamilton Health Sciences Corporation
Enrollment
170
Locations
1
Primary Endpoint
Liebowitz Social Anxiety Scale [LSAS] (mean change from baseline)
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

Selective serotonin reuptake inhibitors (SSRIs) including sertraline have been found to be effective in the treatment of generalized social phobia (GSP). However, virtually all of the current treatment studies with medicines, including the SSRIs, have excluded patients with social phobia who have other co-occurring conditions. In fact, 80% of individuals suffering with primary social phobia have at least one other anxiety. This study will evaluate the safety and efficacy of sertraline in the treatment of generalized social phobia with co-occurring anxiety and mood disorders.

Registry
clinicaltrials.gov
Start Date
July 2002
End Date
January 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Outpatient with primary Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) GSP plus at least one of the following comorbid DSM-IV anxiety disorders:
  • panic disorder with agoraphobia
  • obsessive compulsive disorder
  • major depressive disorder
  • generalized anxiety disorder
  • Score on LSAS \> 50
  • Score on MADRS \< 25

Exclusion Criteria

  • Any other primary AXIS-I diagnosis
  • Criteria for alcohol/substance abuse/dependence
  • History (Hx) of bipolar disorder, schizophrenia or other psychotic disorder
  • A comorbid Axis II cluster A personality disorder
  • Current increased risk of concomitant suicide
  • Allergy/previous intolerance during an adequate trial (50mg/day for minimum of 4 weeks) of sertraline
  • Participation in any clinical trial 30 days prior to entering the study
  • Unable to tolerate being free of/shows signs of withdrawal from benzodiazepines for 4 weeks
  • Hx of seizures
  • Thyroid problems

Arms & Interventions

1

Sertraline

Intervention: Sertraline

2

Placebo

Intervention: Placebo

Outcomes

Primary Outcomes

Liebowitz Social Anxiety Scale [LSAS] (mean change from baseline)

Time Frame: 16 weeks

Clinical Global Impression - Improvement ≤ 2

Time Frame: 16 weeks

Secondary Outcomes

  • Social Phobia Scale(16 weeks)
  • Mean change from baseline on the following scales: Quality of Life and Employment Satisfaction Questionnaire(16 weeks)
  • Sheehan Disability Scale(16 weeks)
  • Brief Social Phobia Scale(16 weeks)
  • Penn State Worry Questionnaire(16 weeks)
  • Panic and Agoraphobia Scale(16 weeks)
  • Davidson Trauma Scale(16 weeks)
  • Social Anxiety Spectrum Self-Report (SHY-SR)(16 weeks)
  • Yale-Brown Obsessive Compulsive Scale(16 weeks)
  • Montgomery-Asberg Depression Rating Scale (MADRS)(16 weeks)

Study Sites (1)

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