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What to know before participating
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Study clarity
Things to check before joining
Study start dateMarch 2010
Recruitment status
Completed
Enrollment listed in the registry
80
Sponsor
Columbia Northwest Pharmaceuticals
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
From 18 Years to 75 Years
Official registry ID
NCT01189812
Official title
A Randomized, Double-Blind, Placebo-Controlled, Fixed-Dose Study to Assess the Safety and Efficacy of Citalopram in Combination With Lithium or Placebo in the Treatment of Symptoms in Patients With Depressive Mood Disorders
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Study ID: NCT01189812. We help you review the study, but cannot decide medical eligibility.
Recruitment & locations
Completed
San Diego · Bellevue
Registry details
Registry conditions (original wording)
Major Depressive Disorder; Dysthymia; Depression Not Otherwise Specified; Borderline Personality Disorder
A listed location does not confirm current availability.
FAQ
Questions about this study
Who is behind this study?
The study sponsor is Columbia Northwest Pharmaceuticals.
Does this study involve medication?
Yes. The study involves medication, including Lithium Carbonate, Placebo and Citalopram.
Who can participate?
Listed age limits: 18 years to 75 years.
Is this study still recruiting?
The registry lists this study as completed.
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