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An 8-week, Randomized, Double-Blind, Placebo-Controlled Trial of Seroquel SR Co-administration for SSRI-Resistant, Comorbid Panic Disorder
The primary objective of this study is to test the hypothesis that a SSRI plus quetiapine SR (Seroquel SR) will result in superior early (first 1-3 weeks of treatment) stabilization of panic symptoms in SSRI-resistant, comorbid Panic Disorder patients versus a SSRI plus placebo.
Details
| Lead sponsor | Indiana University |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 26 |
| Start date | 2008-02 |
| Completion | 2011-12 |
Conditions
- Panic Disorder
Interventions
- quetiapine XR
- placebo
Primary outcomes
- Change in Mean Total Panic Disorder Severity Scale (PDSS) Scores — Baseline and the end of 8 weeks of treatment
Possible total scores on the PDSS range from 0-28. The outcome measure represents the change, between baseline and the end of 8 weeks of treatment, in the the total PDSS scores. Lower scores indicate less severe panic disorder symptoms. A negative mean change in the scores at the end of 8 weeks represents a decrease in severity of panic disorder symptoms.
Countries
United States