NCT Number: NCT00216554
The Safety and Efficacy of Risperidone as Adjunctive Therapy to Mood Stabilizers in the Long-term Treatment of Bipolar Mania
The purpose of this study is to evaluate effect of risperidone as a long-term combination therapy to mood stabilizers in the treatment of bipolar mania
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Notify MeKey information
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
About this study
The use of mood stabilizers such as lithium and carbamazepine is known to be effective for preventing and treating bipolar disorder. But the use of antipsychotic drugs is more effective in patients suffering severe episodes of mania as it elicits behavioral changes and spurs the effects of mood stabilizers. Antipsychotic drugs are used for patients who failed to respond to mood stabilizers or for the acute management of manic episodes associated with bipolar disorders.
This study aims to evaluate the safety and efficacy of risperidone as an adjunctive therapy to mood stabilizers in the long-term treatment (6months) of bipolar disorder using various assessment instruments, including the Young Mania Rating Scale. The Simpson-Angus Rating Scale will be also employed to assess the presence of extrapyramidal side effects and other adverse events. The patients will receive orally 0.5, 1, 2 mg risperidone tablet once daily for 6 months
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- In- or out-patient
- Diagnosis of bipolar I disorder
- most recent episode manic with or without psychotic features
- YMRS > 20 (manic)
- Need antipsychotic combination on the basis of clinicians' experience
Exclusion criteria
- Rapid cycling
- Risk of suicide or violence
- History of Substance dependence within 3 months
- Comorbidities
- Unstable medical illness
- Previous sensitivity history to risperidone
- Pregnant woman or those without proper contraception
- History of clozapine and one cycle of depot use prior to entry
- History of treatment resistance: at least two mood stabilizers
- Prior history of active treatment with risperidone
- As for patients having wash-out period, patients that show 25% or more decrease in YMRS at baseline as compared to that at enrollment time, should be excluded.
Treatment and study plan
Primary outcomes
-
The change in YMRS score from baseline at 6 months
Secondary outcomes
-
The change from baseline in Clinical Global Impression-Severity (CGI-S) score at 6 months; The change from baseline in HAMD score at 6 months
Sponsors and collaborators
Lead sponsor
Janssen Korea, Ltd., Korea
Industry
Registry information
Official study title
A Multicenter, Open-Label Study to Evaluate Safety and Efficacy of Risperidone as Adjunctive Therapy to Mood Stabilizers in the Long-term Treatment of Bipolar Mania
Important dates
- Study start
- 2004
- Study completion
- 2006
- First posted
- Sep 22, 2005
- Registry last updated
- Jan 24, 2011
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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