Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:00 PM
Ignite Modification Date:
2025-12-24 @ 3:00 PM
NCT ID:
NCT00612859
Eligibility Criteria:
Inclusion Criteria:
* Male or female outpatients between 18 and 70 years old inclusive;
* symptoms of social anxiety disorders (generalized type) present for at least 1 year prior to Selection Visit;
* had a score of \>=60 on the LSAS at the Selection Visit and at the Randomization Visit. Additionally, the clinician's gloal impression of change score must have been \>= 2 at the Randomization Visit;
* had a telephone where they could be directly contacted.
Exclusion Criteria:
* History of autism or Asperger's Disease;
* had another primary axis I disorder or fulfilled diagnostic and statistical manual of mental disorders-4th edition (DSM-IV) criteria in the 6 months prior to Screening;
* major depression as measured by a Hamilton Depression Rating Scale (HAM-D-17 items) total score of \> 17 and/or a suicide subscale score on the HAM-D-17 items of \> 2 at the Selection or Randomization Visit;
* history of electroconvulsive therapy within the prior 3 months;
* history of psychotherapy which was not stable and ongoing for at least 6 months prior to Visit 1;
* clinical history of significantly impaired renal function with an estimated creatinine clearance below 80 mL/min;
* clinically significant medical condition;
* history of any clinically significant allergic condition or allergy to LEV or pyrrolidone derivatives;
* neutrophil count of less than 1800/µL.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT00612859
Study Brief:
Protocol Section:
NCT00612859