NCT00195598
Completed
Phase 3
Pilot Study of Venlafaxine Extended Release (XR) in the Treatment of Panic Disorder (PD) in Comparison to Paroxetine.
Wyeth is now a wholly owned subsidiary of Pfizer0 sites70 target enrollmentJanuary 2005
ConditionsPanic Disorders
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Panic Disorders
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer
- Enrollment
- 70
- Primary Endpoint
- To evaluate the improvement of social function following therapy with Venlafaxine extended release (XR)in the Treatment of Panic Disorder in comparison to Paroxetine.
- Status
- Completed
- Last Updated
- 16 years ago
Overview
Brief Summary
The purpose of this pilot study is to evaluate the improvement in social function following therapy with venlafaxine extended release (XR) in the treatment of panic disorder (PD) in comparison to paroxetine. An additional purpose of this pilot study is to obtain the tolerability of using venlafaxine extended release (XR) in the treatment of panic disorder (PD) in comparison to paroxetine.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Meet DSM IV criteria for Panic Disorder (with or without agoraphobia) for at least 3 months before study day
- •Have a minimum of 8 full-symptom panic attacks during the 4 weeks before the screening visit.
- •Provide a written informed consent
Exclusion Criteria
- •Treatment with Venlafaxine within 6 months of study day 1, as well Paroxetine
- •Known hypersensitivity to Venlafaxine or related compounds as well to Paroxetine.
- •Psychopharmacologic drugs within 14 days of study day 1
Outcomes
Primary Outcomes
To evaluate the improvement of social function following therapy with Venlafaxine extended release (XR)in the Treatment of Panic Disorder in comparison to Paroxetine.
Secondary Outcomes
- Obtain the tolerability of using Venlafaxine extended release (XR) in the treatment of Panic Disorder in comparison to Paroxetine.
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