CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 356 enrolled
Drug / intervention
Quetiapine fumarate XR +2 moredrug
Likely dose
Quetiapine fumarate XR 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/NCT00931723
NCT00931723Phase 4Completed

An International, Multicenter, Double-blind, Randomized, Placebo-controlled, Phase IV Study of the Safety and Efficacy of Lithium Versus Placebo as an Add on to SEROQUEL XR (Quetiapine Fumarate) in Adult Patients With Acute Mania

AstraZeneca·interventional·Posted Jul 2, 2009·Updated Apr 19, 2012

In Brief

A Phase 4 clinical trial evaluating Quetiapine fumarate XR, Lithium, and 1 other intervention for Acute Mania. Completed, enrolled 356 participants across 65 sites in 9 countries.

Detailed Summary

The purpose of this study is to determine if lithium 600-1800 mg/day is effective when added to quetiapine fumarate extended release (quetiapine XR or SEROQUEL® XR) 400-800 mg/day in treating acute mania and if so, how it compares with placebo (a non-active capsule, like a sugar pill, that looks like lithium).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAcute Mania
CountriesBelgium, Bulgaria, Germany, India, Israel, Poland, Russia, South Africa, Ukraine
CollaboratorsQuintiles, Inc.

Timeline

Phase 4CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJul 2, 2009
Enrollment StartJun 1, 2009
Primary CompletionNov 1, 2010
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 17 years ago

Interventions

Quetiapine fumarate XRdrug

Oral treatment, once daily, Day 1 = 300 mg, Day 2 and thereafter 600 mg. Dose might be adjusted as from Day 3 by the discretion of the investigator.

Lithiumdrug

Oral treatment, twice daily, Days 1 and 2 = 600 mg/day, Days 3-8 = 900 mg/day. Dose adjustment from day 9 to end of study will be at the discretion of the investigator.

Placebodrug

Oral treatment twice daily.