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| Sponsored by: |
Department of Veterans Affairs |
| Information provided by: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00018733 |
Purpose
This study will be measuring changes in depressive symptoms over a 7 week time period. Double-blind placebo controlled trial using the pharmacologic agents Paroxetine or Desipramine.
| Condition | Intervention |
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Depression |
Drug: paroxetine Drug: Desipramine |
| MedlinePlus related topics: | Antidepressants Depression |
| Drug Information available for: | Desipramine Desipramine hydrochloride Paroxetine Paroxetine hydrochloride Paroxetine Mesylate |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Pharmacodynamics Study |
| Official Title: | Biological Aspects of Depression and Antidepressant Drugs |
Eligibility
| Ages Eligible for Study: | 21 Years to 69 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Contacts and Locations
More Information
| Study ID Numbers: | MHBS-031-99F |
| First Received: | July 3, 2001 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00018733 |
| Health Authority: | United States: Federal Government |
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