Viewing Study NCT00343707



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00343707
Status: COMPLETED
Last Update Posted: 2016-09-15
First Post: 2006-06-21

Brief Title: PET Positron Emission TomographyPublic Speaking Study With A Combination Of 2 Medications In Social Anxiety Patients
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: A Double-blind Triple Dummy Placebo-controlled Randomised Parallel Group Positron Emission Tomography Study to Investigate the Effects of a 8 Week Administration of GW597599 and Paroxetine Either Alone or in Combination on Regional Cerebral Blood Flow During a Public Speaking Test in Subjects Affected by Social Phobia
Status: COMPLETED
Status Verified Date: 2016-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This six-arm study is being conducted to measure the effect of a combination of paroxetine and vestipitant on the arousal induced by public speaking in Seasonal Effective Disorder SAD patients using functional brain imaging readouts ie WATWave Analysis Technology PETPositron Emission Tomography after one or eight weeks of treatment The effect of paroxetine alone after one or eight weeks of treatment will also be measured
Detailed Description: A double-blind double dummy placebo-controlled randomised parallel group positron emission tomography study to investigate the effects of a 8 week administration of vestipitant and paroxetine in combination or paroxetine alone on regional cerebral blood flow during a public speaking test in subjects affected by social anxiety disorder

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None