Improving Treatment Outcomes in Pharmacotherapy of Generalized Social Anxiety Disorder
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ClinicalTrials.gov Identifier: NCT00282828 |
Recruitment Status :
Completed
First Posted : January 27, 2006
Results First Posted : October 14, 2013
Last Update Posted : October 14, 2013
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Social Phobia | Drug: Sertraline Drug: Venlafaxine Drug: Placebo Drug: Clonazepam | Phase 4 |
Generalized social anxiety disorder (GSAD) is one of the most common psychiatric disorders, and often causes significant distress and dysfunction in affected individuals. Although currently available treatments for GSAD are effective, most individuals have residual symptoms after initial psychosocial or psychopharmacologic intervention. Further treatment is necessary for such individuals, but sufficient research has not been done to guide clinicians on what the safest and most effective next step may be. This study will compare the effectiveness of either combining clonazepam or placebo with sertraline or completely switching to venlafaxine in treating GSAD in individuals who have not responded to treatment with sertraline. This study will also examine predictors of treatment response, including factors such as age at disease onset, duration of illness, comorbidities, and genes that influence serotonin and catecholamine metabolism.
Participants in this double-blind study will first partake in an initial 10-week phase in which they will be treated with sertraline. Participants who do not respond to sertraline treatment will proceed to phase two of the study, in which they will be randomly assigned to one of three treatment groups. One group will receive both sertraline and clonazepam, another group will receive both sertraline and placebo, and the third group will receive only venlafaxine. All treatments will continue for 12 weeks. Sertraline and venlafaxine are both FDA-approved for the treatment of GSAD. Clonazepam is widely used for the treatment of anxiety, but is not FDA-approved for the treatment of GSAD. All participants will attend weekly study visits at Weeks 1, 2, 4, 6, 8, and 10. Participants who continue into phase two will attend weekly study visits at Weeks 11-14, 16, 18, 20, and 22. Symptom remission rates and post-treatment social phobia severity will be assessed at Week 22.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 397 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Improving Outcomes in Pharmacotherapy of Social Phobia |
Study Start Date : | March 2006 |
Actual Primary Completion Date : | December 2011 |
Actual Study Completion Date : | December 2011 |

Arm | Intervention/treatment |
---|---|
Experimental: Sertraline & Clonazepam
Phase I non-responders randomized to this group remained on sertraline at the same dose level as at entry into Phase 2 with the addition of clonazepam up to 3.0mg per day. Dosing was flexible, permitting clinicians to slow or suspend the titration of the medication because of side effects or response, but patients had to receive no less than 0.5mg of clonazepam per day in order to remain in the study. |
Drug: Sertraline Drug: Clonazepam |
Experimental: Venlafaxine
Phase I non-responders randomized to this group switched to venlafaxine with flexible titration up to 225 mg per day. Dosing was flexible, permitting clinicians to slow or suspend the titration of the medication because of side effects or response, but patients had to receive no less than 75 mg venlafaxine per day in order to remain in the study. |
Drug: Venlafaxine |
Experimental: Sertraline & Placebo
Phase I non-responders randomized to this group remained on sertraline at the same dose level as at entry into Phase 2 with the addition of placebo. Dosing was flexible, permitting clinicians to slow or suspend the titration of the medication because of side effects or response, but patients had to receive no less than 1 capsule of placebo per day in order to remain in the study. |
Drug: Sertraline Drug: Placebo |
- Rates of Remission (LSAS≤30) After 12 Weeks of Randomized Treatment During Phase II, Among Phase I Non-responders [ Time Frame: Measured at Week 22 (Endpoint) ]The Liebowitz Social Anxiety Scale (LSAS) is a 24-item scale assessing fear and avoidance in social and performance situations; it is widely used in studies of pharmacological treatment of Generalized Social Anxiety Disorder (GSAD). Scores on the LSAS range from 0 to 144, with higher scores indicating greater pathology.
- Post-treatment Social Phobia Severity as Defined by Endpoint LSAS Scores [ Time Frame: Change from Week 10 to Week 22 ]The Liebowitz Social Anxiety Scale (LSAS) is a 24-item scale assessing fear and avoidance in social and performance situations; it is widely used in studies of pharmacological treatment of Generalized Social Anxiety Disorder (GSAD). We analyzed the overall change in LSAS (last Phase II LSAS minus Week 10 LSAS). Higher numbers reflect greater drops in social anxiety disorder severity. Scores on the LSAS range from 0 to 144, with higher scores indicating greater pathology.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00282828
United States, California | |
University of California San Diego | |
La Jolla, California, United States, 92093 | |
United States, Massachusetts | |
Center for Anxiety and Traumatic Stress Disorders | |
Boston, Massachusetts, United States, 02116 | |
Canada, Ontario | |
McMaster University Medical Centre Anxiety Disorders Clinic | |
Hamilton, Ontario, Canada, L8N 3Z5 |
Principal Investigator: | Mark H. Pollack, MD | Massachusetts General Hospital | |
Principal Investigator: | Murray B. Stein, MD, MPH | University of California San Deigo | |
Principal Investigator: | Michael Van Ameringen, MD, FRCPC | Anxiety Disorders Clinic McMaster University Medical Centre |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Mark H. Pollack, Principal Investigator, Massachusetts General Hospital |
ClinicalTrials.gov Identifier: | NCT00282828 |
Other Study ID Numbers: |
R01MH070919 ( U.S. NIH Grant/Contract ) R01MH070919 ( U.S. NIH Grant/Contract ) PA-01-123 DSIR 83-ATAS |
First Posted: | January 27, 2006 Key Record Dates |
Results First Posted: | October 14, 2013 |
Last Update Posted: | October 14, 2013 |
Last Verified: | August 2013 |
Social Anxiety Disorder Pharmacotherapy Genetics Treatment Refractory |
Anxiety Disorders Phobic Disorders Phobia, Social Mental Disorders Clonazepam Sertraline Venlafaxine Hydrochloride Antidepressive Agents Psychotropic Drugs Serotonin Uptake Inhibitors Neurotransmitter Uptake Inhibitors |
Membrane Transport Modulators Molecular Mechanisms of Pharmacological Action Neurotransmitter Agents Serotonin Agents Physiological Effects of Drugs Serotonin and Noradrenaline Reuptake Inhibitors Antidepressive Agents, Second-Generation Anticonvulsants GABA Modulators GABA Agents |