This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.This is a twelve-week placebo controlled study of paroxetine and venlafaxine extended release. Paroxetine and venlafaxine are drugs that have been approved by the FDA and are available by prescriptions. Paroxetine and venlafaxine have been shown to be effective in treating depression in the general population. There is a 2 in 3 chance that a participant will receive active drug and a 1 in 3 chance that they will receive placebo. This will be decided randomly, like flipping a coin. This is a double blind study, so neither the participant nor the investigator will know if they are receiving placebo or active drug. Only the pharmacist dispensing the medication will know which study treatment each participant will receive.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR016500-07
Application #
7718059
Study Section
Special Emphasis Panel (ZRR1-CR-3 (02))
Project Start
2008-03-01
Project End
2009-02-28
Budget Start
2008-03-01
Budget End
2009-02-28
Support Year
7
Fiscal Year
2008
Total Cost
$5,539
Indirect Cost
Name
University of Maryland Baltimore
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
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