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CompletedNCT01189812

Safety and Efficacy of Citalopram for depression

This study is completed in the United States. It is testing safety and Efficacy of Citalopram for depression.

Personality disorders, Depression, ...DrugFrom 18 Years to 75 Years
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 75 years.

Listed locations
San Diego, United States · Bellevue, United StatesSee all locations and recruitment

Compensation and expense reimbursement have not been verified for this summary.

What to know before participating

A point to clarify

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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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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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