CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 80 enrolled
Drug / intervention
Lithium Carbonate +2 moredrug
Likely dose
Lithium Carbonate 300 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01189812
NCT01189812Phase 2Completed

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

Columbia Northwest Pharmaceuticals·interventional·Posted Aug 27, 2010·Updated Aug 24, 2011

In Brief

A Phase 2 clinical trial evaluating Lithium Carbonate, Placebo, and 1 other intervention for Major Depressive Disorder and 3 related conditions. Completed, enrolled 80 participants across 2 sites.

Detailed Summary

The investigators hypothesize that patients receiving citalopram in combination with lithium will have a greater reduction in depressive symptoms than patients receiving citalopram in combination with placebo.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedAug 27, 2010
Enrollment StartMar 1, 2010
Primary CompletionJan 1, 2011
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 15.8 years ago

Interventions

Lithium Carbonatedrug

300 mg one time per day for 4 weeks

Placebodrug

Take one time daily for 4 weeks

Citalopramdrug

All patients will be administered Citalopram 20 mg to to be taken once daily, by mouth for the duration of the double-blind treatment phase (4 weeks)