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Efficacy of Quetiapine in Generalised Social Anxiety Disorder

Efficacy of Quetiapine in Generalised Social Anxiety Disorder, a Double-blind, Placebo-controlled Study

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00302770
Enrollment
50
Registered
2006-03-15
Start date
2006-06-30
Completion date
2006-12-31
Last updated
2011-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Social Anxiety Disorder

Keywords

Patients with SAD

Brief summary

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

Interventions

DRUGquetiapine

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Change on Lebowitz Social Anxiety Scale (LSAS) from baseline to endpoint

Secondary

MeasureTime frame
Number of responders, time to onset of response of sustained response to treatment

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026