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| Sponsor: | 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 |
|---|---|
|
Depression |
Drug: paroxetine Drug: Desipramine |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Pharmacodynamics Study Masking: Double-Blind Primary Purpose: Treatment |
| 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
| ClinicalTrials.gov Identifier: | NCT00018733 History of Changes |
| Other Study ID Numbers: | MHBS-031-99F |
| Study First Received: | July 3, 2001 |
| Last Updated: | January 20, 2009 |
| Health Authority: | United States: Federal Government |
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Depression |
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Depression Depressive Disorder Behavioral Symptoms Mood Disorders Mental Disorders Antidepressive Agents Desipramine Paroxetine Psychotropic Drugs Central Nervous System Agents Therapeutic Uses Pharmacologic Actions |
Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Antidepressive Agents, Tricyclic Adrenergic Uptake Inhibitors Adrenergic Agents Neurotransmitter Agents Neurotransmitter Uptake Inhibitors Physiological Effects of Drugs Serotonin Uptake Inhibitors Serotonin Agents Antidepressive Agents, Second-Generation |