Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT00332891 |
Date of registration:
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01/06/2006 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Patients With Generalized Anxiety Disorder
ELECTRA |
Scientific title:
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An 8-Week, Double-Blind, Placebo-Controlled, Multicenter Study With Paroxetine (20 mg q24) as Positive Control, Evaluating the Efficacy and Safety of 2 Fixed Doses of SR58611A (175 mg q12 and 350 mg q12) in Outpatients With GAD |
Date of first enrolment:
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March 2006 |
Target sample size:
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508 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT00332891 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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Phase:
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Phase 3
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Countries of recruitment
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Bulgaria
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Croatia
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Czech Republic
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Former Serbia and Montenegro
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Poland
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Serbia
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Contacts
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Name:
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ICD CSD |
Address:
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Telephone:
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Email:
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Affiliation:
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Sanofi |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients suffering from generalized anxiety disorder (GAD) as defined by DSM-IV-TR
criteria and confirmed by the Mini International Neuropsychiatric Interview (MINI)
plus GAD Module
- Total score on the 14-item Hamilton Anxiety Rating Scale (HAM-A) equal or above 20.
Exclusion Criteria:
- Patients with a diagnosis of Major Depressive Disorder as defined by DSM-IV-TR within
6 months of study entry.
- Patients with a Montgomery-Asberg Depression Rating Scale (MADRS) total score of 18
or higher at screening or baseline visits.
- Patients having a moderate to high current risk for suicide.
- Patients with other current anxiety disorder assessed with the MINI: agoraphobia,
social phobia, panic disorder, obsessive-compulsive disorder, post-traumatic stress
disorder, acute stress disorder.
- Patients with a lifetime history according to the MINI of: bipolar disorders,
psychotic disorders, antisocial personality disorder.
- Patients with severe or unstable concomitant medical conditions according to the
Investigator's judgment.
- Females who are pregnant or lactating.
- Female patients of childbearing potential must use an effective method of birth
control during the entire study period.
- Patients with positive test for any illicit drug included in the urine drug screen.
- Participation in a clinical trial of an experimental therapy within 3 months prior to
screening
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Anxiety Disorders
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Intervention(s)
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Drug: SR58611A
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Primary Outcome(s)
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The primary outcome of the study is the change from baseline to Day 56 of treatment in the Hamilton Anxiety Rating Scale (HAM-A) total score.
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Secondary Outcome(s)
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The main secondary outcomes are the changes from baseline to Day 56 of treatment in the CGI Severity of Illness Score, percentage of patients with HAM-A treatment response and change from baseline in the HAM-A somatic and psychic anxiety factor scores.
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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