Changes of Cerebral Glucose Metabolism After 12 Weeks of Paroxetine Treatment in Panic Disorder
NCT ID: NCT00767754
Last Updated: 2011-07-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
37 participants
INTERVENTIONAL
2007-01-31
2008-12-31
Brief Summary
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The specific aim of this study is to examine the differences in brain activity between responders and nonresponders and to determine the predictor of paroxetine treatment in patients with panic disorder in terms of brain activity.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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paroxetine cr
single arm
Paxil CR
12 week treatment of Paxil(20-40mg)
Interventions
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Paxil CR
12 week treatment of Paxil(20-40mg)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* less than 17 on the HAM-D
20 Years
60 Years
ALL
Yes
Sponsors
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Samsung Medical Center
OTHER
Responsible Party
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Department of Psychiatry, Samsung Medical Center
Principal Investigators
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Bum-Hee Yu, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Samsung Medical Center
Locations
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Samsung Medical Center
Seoul, , South Korea
Countries
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Other Identifiers
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SMC IRB 2006-07-091
Identifier Type: -
Identifier Source: org_study_id
NCT00515749
Identifier Type: -
Identifier Source: nct_alias
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