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Sponsored by: |
Merck |
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Information provided by: | Merck |
ClinicalTrials.gov Identifier: | NCT00539578 |
The purpose of the study is to examine the safety and efficacy of MK0777 during treatment for Generalized Anxiety Disorder.
Condition | Intervention | Phase |
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Generalized Anxiety Disorder |
Drug: MK0777 Drug: Comparator: placebo (unspecified) |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | A Double-Blind, Mulit-Center, Placebo-Controlled, Flexible-Dose Replicate Study of MK0777 Gel Extrusion Module (GEM) 3 mg B.I.D. to 8 mg B.I.D. in the Treatment of Outpatients With Generalized Anxiety Disorder |
Enrollment: | 270 |
Study Start Date: | October 2002 |
Study Completion Date: | February 2003 |
Primary Completion Date: | February 2003 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | 18 Years to 70 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Merck & Co., Inc. ( Executive Vice President, Clinical and Quantitative Sciences ) |
Study ID Numbers: | 2007_622, MK0777-022 |
Study First Received: | October 1, 2007 |
Last Updated: | May 19, 2008 |
ClinicalTrials.gov Identifier: | NCT00539578 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Anxiety Disorders Mental Disorders |
Pathologic Processes Disease Anxiety Disorders Mental Disorders |