Efficacy of Quetiapine in Generalised Social Anxiety Disorder

NCT ID: NCT00302770

Last Updated: 2011-01-27

Study Results

Results pending

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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Recruitment Status

TERMINATED

Clinical Phase

PHASE3

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-06-30

Study Completion Date

2006-12-31

Brief Summary

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This trial will explore the efficacy of quetiapine in Social Anxiety Disorder, generalized type. The following elements of response will be tested: number of responders to treatment, time to response, effect size as measured with the LSAS

Detailed Description

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Conditions

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Social Anxiety Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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quetiapine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Written Confirmed Consent,
* All patients meet the DSM IV criteria for generalized social anxiety disorder,
* A score ≥ 60 on the LSAS,
* male and female aged between 18 and 65 years

Exclusion Criteria

* Presence of any primary axis I diagnosis other than social anxiety disorder according to DSM-IV,
* alcohol and/or substance abuse according to DSM-IV criteria within the last 12 months,
* any personality disorder as the primary diagnosis, with the exception of avoidant personality disorder,
* patients at risk of suicide
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Principal Investigators

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AstraZeneca Netherlands Medical Director, MD

Role: STUDY_DIRECTOR

AstraZeneca

Locations

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Research Site

Utrecht, , Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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D1449C00008

Identifier Type: -

Identifier Source: org_study_id

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