A Study of MK0777 in the Treatment of Outpatients With Generalized Anxiety Disorder
This study has been completed.
Sponsor:
Merck
Information provided by:
Merck
ClinicalTrials.gov Identifier:
NCT00543920
First received: October 5, 2007
Last updated: October 12, 2007
Last verified: October 2007
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Purpose
The study will look at the effect of MK0777on reducing anxiety in subjects with general anxiety disorder.
This is an early phase trial and some specific protocol information is in progress and not publicly available at this time. (Full information is available to trial participants).
| Condition | Intervention | Phase |
|---|---|---|
|
Anxiety Disorders |
Drug: MK0777 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
Resource links provided by NLM:
Further study details as provided by Merck:
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Diagnosis of General Anxiety Order
Exclusion Criteria:
- Women who are pregnant or breast-feeding
- History of severe drug reaction
- History of severe drug withdrawal symptoms such as seizures or delirium
- Disease of cardiovascular system
- Disease of the liver, kidneys, endocrine system, metabolic system or eyes
- History of seizures or seizure disorder
- History of drug or alcohol abuse
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00543920 History of Changes |
| Other Study ID Numbers: | 2007_633 |
| Study First Received: | October 5, 2007 |
| Last Updated: | October 12, 2007 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Anxiety Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 23, 2013