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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 |
|---|---|
|
Depression |
Drug: paroxetine Drug: Desipramine |
| 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 |
| Study First Received: | July 3, 2001 |
| Last Updated: | January 20, 2009 |
| ClinicalTrials.gov Identifier: | NCT00018733 History of Changes |
| Health Authority: | United States: Federal Government |
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Depression |
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Neurotransmitter Agents Depression Adrenergic Agents Psychotropic Drugs Depressive Disorder Desipramine Serotonin Uptake Inhibitors Paroxetine |
Serotonin Behavioral Symptoms Antidepressive Agents, Tricyclic Mental Disorders Mood Disorders Antidepressive Agents, Second-Generation Antidepressive Agents |
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Neurotransmitter Uptake Inhibitors Neurotransmitter Agents Depression Adrenergic Agents Molecular Mechanisms of Pharmacological Action Adrenergic Uptake Inhibitors Physiological Effects of Drugs Psychotropic Drugs Enzyme Inhibitors Depressive Disorder Desipramine Serotonin Uptake Inhibitors |
Paroxetine Pharmacologic Actions Antidepressive Agents, Tricyclic Behavioral Symptoms Serotonin Agents Mental Disorders Therapeutic Uses Mood Disorders Antidepressive Agents, Second-Generation Central Nervous System Agents Antidepressive Agents |