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Generated: June 16, 2019

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CLINICAL TRIALS PROFILE FOR LITHIUM CARBONATE

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Clinical Trials for Lithium Carbonate

Trial ID Title Status Sponsor Phase Summary
NCT00000369 Maintenance Therapies in Bipolar Disorders Completed University of Pittsburgh Phase 3 The purpose of this study is to see if adding a regimen of individualized psychotherapy can help bipolar I patients who are on lithium. While having a manic or depressed episode patients will be assigned randomly (like tossing a coin) to receive appropriate medication either with or without additional individual psychotherapy. If a patient responds well, he/she will again be assigned randomly to receive further preventative treatment in which medication will be managed either with continued medication clinic visits alone or with additional individual psychotherapy (the patient may not receive the same additional treatment this time). Patient response to treatment will be evaluated throughout the study. If manic/depressive symptoms return at any point during the study, the patient will be treated with appropriate medication and will continue the study. An individual may be eligible for this study if he/she: Has Bipolar I disorder, is experiencing a manic or depressed episode at the time of study entry, and is at least 18 years old.
NCT00000439 Drug Treatment for Alcoholics With Bipolar Disorder Completed University of Pittsburgh Phase 2 The purpose of this study is to test the effectiveness of sodium valproate (Depacon) in treating individuals with alcohol dependence and comorbid bipolar disorder.
NCT00000439 Drug Treatment for Alcoholics With Bipolar Disorder Completed National Institute on Alcohol Abuse and Alcoholism (NIAAA) Phase 2 The purpose of this study is to test the effectiveness of sodium valproate (Depacon) in treating individuals with alcohol dependence and comorbid bipolar disorder.
NCT00005015 Treatment of Depression in Youth With Bipolar Disorders Terminated National Institute of Mental Health (NIMH) Phase 3 THIS STUDY HAS BEEN DISCONTINUED. The study is designed to evaluate the safety and efficacy of fluoxetine for treating children and adolescents with Bipolar Disorder who are experiencing an episode of major depression while being treated with a mood stabilizer. The study involves a 2-week assessment period. Patients who are on stable, therapeutic doses of lithium or valproate and continue to have depression will be randomized to a 12-week treatment of fluoxetine or placebo. Those who respond favorably to treatment will be followed openly for an 18-week continuation phase.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Lithium Carbonate

Condition Name

Condition Name for Lithium Carbonate
Intervention Trials
Bipolar Disorder 17
Major Depressive Disorder 4
Amyotrophic Lateral Sclerosis 3
Spinal Cord Injuries 3
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Condition MeSH

Condition MeSH for Lithium Carbonate
Intervention Trials
Bipolar Disorder 23
Disease 11
Depressive Disorder 6
Depression 6
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Clinical Trial Locations for Lithium Carbonate

Trials by Country

Trials by Country for Lithium Carbonate
Location Trials
United States 48
China 13
Canada 7
Italy 3
Israel 3
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Trials by US State

Trials by US State for Lithium Carbonate
Location Trials
Pennsylvania 6
New York 6
Ohio 5
Texas 3
Maryland 3
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Clinical Trial Progress for Lithium Carbonate

Clinical Trial Phase

Clinical Trial Phase for Lithium Carbonate
Clinical Trial Phase Trials
Phase 4 11
Phase 3 9
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Lithium Carbonate
Clinical Trial Phase Trials
Completed 32
Recruiting 13
Terminated 9
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Clinical Trial Sponsors for Lithium Carbonate

Sponsor Name

Sponsor Name for Lithium Carbonate
Sponsor Trials
National Institute of Mental Health (NIMH) 5
Roxane Laboratories 4
National Cancer Institute (NCI) 4
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Sponsor Type

Sponsor Type for Lithium Carbonate
Sponsor Trials
Other 79
NIH 16
Industry 11
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Serving hundreds of leading biopharmaceutical companies globally:

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