Improving Treatment Outcomes in Pharmacotherapy of Generalized Social Anxiety Disorder

Completed · Phase 4 · Has a placebo group

Conditions studied: Social Phobia

In brief

This study will compare the effectiveness of either adding clonazepam or placebo to standard treatment or switching to venlafaxine in treating generalized social anxiety disorder in individuals who have not responded to treatment with sertraline.

Key facts

Study ID

NCT00282828

Run by

Massachusetts General Hospital

People needed

397

Starts

2006-03-01

Expected to finish

2011-12-01

Last updated by the study team

2013-10-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Primary psychiatric diagnosis of GSAD as defined by DSM-IV criteria and a score above 60 on the LSAS
• Agrees to use an effective form of contraception throughout the study

You may not qualify if…

• Clinically significant abnormalities found upon physical examination, electrocardiogram, and laboratory tests
• History of more than two unsuccessful, adequate treatment trials, indicated by a lack of response to over 10 weeks of any of the following: SSRIs (e.g., 40 mg of paroxetine or its equivalent per day); benzodiazepine (e.g. at least 2.5 mg of clonazepam per day) plus antidepressant (adequate dose as above); monoamine oxidase inhibitors (e.g., 60 mg of phenelzine or its equivalent per day); or a single failed trial of over 10 weeks of venlafaxine ( at least 150 mg per day)
• Pregnant or breastfeeding
• Simultaneous use of other psychotropic medications, with the exception of psychostimulants to treat ADHD; participants must discontinue regular benzodiazepine or antidepressant therapy at least two weeks (5 weeks for fluoxetine) prior to study entry; beta-blockers must be discontinued unless they are indicated medically (e.g., for hypertension)
• DSM-IV diagnosis of any of the following: lifetime history of schizophrenia or any other psychosis, mental retardation, organic medical disorder, bipolar disorder, or obsessive compulsive disorder; eating disorder in the past 6 months; alcohol or substance abuse in the past 3 months or dependence within the past 6 months (entry of participants with major depression, dysthymia, panic disorder, generalized anxiety disorder, or post-traumatic stress disorder will be permitted if the social anxiety disorder is judged to be the predominant disorder)
• Significant suicidal ideation as indicated by a score greater than 3 on the Montgomery-Asberg Depression Rating Scale or suicidal behaviors within 6 months prior to study entry
• Significant personality dysfunction that could interfere with study participation
• Serious medical illness or instability for which hospitalization may be likely during the study
• Seizure disorders, with the exception of a childhood history of isolated, non-recurrent febrile seizures
• Any concurrent psychotherapy initiated within 3 months of study entry, or ongoing psychotherapy of any duration directed specifically toward treatment of GSAD (prohibited psychotherapy includes cognitive behavioral therapy or psychodynamic therapy that focuses on exploring specific, dynamic causes of the phobic symptomatology and that provides management skills; general supportive therapy for more than 3 months is acceptable)

Where it is running

• University of California San Diego — La Jolla, California, United States
• Center for Anxiety and Traumatic Stress Disorders — Boston, Massachusetts, United States
• McMaster University Medical Centre Anxiety Disorders Clinic — Hamilton, Ontario, Canada

Full record on ClinicalTrials.gov

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