- Trials with a EudraCT protocol (192)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
192 result(s) found for: Psychosis.
Displaying page 1 of 10.
EudraCT Number: 2007-003035-22 | Sponsor Protocol Number: ACP-103-015 | Start Date*: 2008-11-05 | |||||||||||
Sponsor Name:ACADIA Pharmaceuticals Inc. | |||||||||||||
Full Title: A Multi-Center, Open-Label Extension Study to Examine the Safety and Tolerability of ACP-103 in the Treatment of Psychosis in Parkinson’s Disease | |||||||||||||
Medical condition: Psychosis in Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) SE (Completed) BE (Completed) AT (Completed) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003512-12 | Sponsor Protocol Number: ACP-103-041 | Start Date*: 2017-07-21 | |||||||||||
Sponsor Name:ACADIA Pharmaceuticals Inc. | |||||||||||||
Full Title: An Open-Label Extension Study to Examine the Safety and Tolerability of Pimavanserin in the Treatment of Parkinson’s Disease Psychosis | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001606-66 | Sponsor Protocol Number: OLZvsLMT-DB | Start Date*: 2005-06-16 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: OLANZAPINE VS LAMOTRIGINE ADD-ON TO LITHIUM:EFFICACY ON ANXIETY SYMPTOMS IN REMITTING BIPOLAR PATIENTS | |||||||||||||
Medical condition: EFFICACY ON ANXIETY SYMPTOMS IN REMITTING BIPOLAR PATIENTS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000034-42 | Sponsor Protocol Number: 2022-001 | Start Date*: 2022-04-22 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital - Psychiatry, Department of Affective Disorders | ||||||||||||||||||
Full Title: The Estimated 12-Hour Serum Lithium Level Pilot Study | ||||||||||||||||||
Medical condition: Bipolar disorder Unipolar Depression | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003051-36 | Sponsor Protocol Number: ACP-103-014 | Start Date*: 2008-09-10 | |||||||||||
Sponsor Name:Acadia Pharmaceuticals Inc | |||||||||||||
Full Title: A Multi-Center, Placebo-Controlled, Double-Blind Trial to Examine the Safety and Efficacy of ACP-103 in the Treatment of Psychosis in Parkinson’s Disease | |||||||||||||
Medical condition: Psychosis in Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) ES (Completed) SE (Prematurely Ended) BE (Completed) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004893-84 | Sponsor Protocol Number: CBD-P | Start Date*: 2019-08-22 | ||||||||||||||||
Sponsor Name:Mental Health Center Glostrup | ||||||||||||||||||
Full Title: Cannabidiol for treatment of non-affective psychosis and cannabis use | ||||||||||||||||||
Medical condition: Non-affective psychosis and lifetime cannabis use | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002906-23 | Sponsor Protocol Number: ACP-103-012 | Start Date*: 2007-11-14 | |||||||||||
Sponsor Name:Acadia Pharmaceuticals Inc | |||||||||||||
Full Title: A Multi-Center, Placebo-Controlled, Double-Blind Trial To Examine the Safety and Efficacy of ACP-103 in the Treatment of Psychosis in Parkinson's Disease | |||||||||||||
Medical condition: Psychosis in Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002608-13 | Sponsor Protocol Number: KCL/KCH-CT2004-1 (26/8/04) | Start Date*: 2005-05-16 |
Sponsor Name:King’s College London & King’s College Hospital | ||
Full Title: Pragmatic Randomised Control Trial of Quetiapine for psychosis in Parkinson’s Disease | ||
Medical condition: Parkinson's Disease with psychosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000465-31 | Sponsor Protocol Number: CannaBiD | Start Date*: 2016-06-29 | |||||||||||||||||||||||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||||||||||||||||||||||
Full Title: Cannabidiol in Bipolar Depression – CannaBiD-Study: An 8-week randomized, double-blind, placebo-controlled clinical trial of Cannabidiol as add-on therapy in bipolar depression | |||||||||||||||||||||||||||||||||
Medical condition: Bipolar disorder, current episode depressed | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022184-35 | Sponsor Protocol Number: ATLAS | Start Date*: 2011-10-04 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: A pragmatic randomised double-blind trial of Antipsychotic Treatment of very LAte-onset Schizophrenia-like psychosis: The ATLAS Trial | |||||||||||||
Medical condition: late-onset schizophrenia-like psychosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001599-23 | Sponsor Protocol Number: SIMPET-1 | Start Date*: 2016-06-27 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Groningen | ||||||||||||||||||||||||||||
Full Title: In Vivo Imaging of Neuroinflammation in Simvastatin-Treated Schizophrenic Patients | ||||||||||||||||||||||||||||
Medical condition: Schizophrenia | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011343-39 | Sponsor Protocol Number: RIS-SCH-4226 | Start Date*: 2009-06-15 | |||||||||||||||||||||||||||||||
Sponsor Name:Janssen-Cilag AB | |||||||||||||||||||||||||||||||||
Full Title: Patient and physician preferences and satisfaction with oral and long-acting injectable long-term antipsychotic treatment for psychotic disorders | |||||||||||||||||||||||||||||||||
Medical condition: Schizophrenia, schizoaffective disorder, delusional disorder, psychotic disorder NOS or any other psychotic disorder patients demanding long term antipsychotic treatment | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003972-42 | Sponsor Protocol Number: A1281198 | Start Date*: 2020-08-21 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, FOUR-WEEK, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP EFFICACY AND SAFETY TRIAL OF FLEXIBLE DOSES OF ORAL ZIPRASIDONE IN CHILDREN AND ADOLESCENTS WITH BIPO... | |||||||||||||
Medical condition: Bipolar Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011253-40 | Sponsor Protocol Number: PQ2 | Start Date*: 2009-04-23 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: Paroxetine or Quetiapine in Addition to Mood Stabilizers in Bipolar Depression | |||||||||||||
Medical condition: Major Depressive Episode in Bipolar Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023740-32 | Sponsor Protocol Number: 2010-023740-32 | Start Date*: 2011-05-18 | |||||||||||
Sponsor Name:Haukeland University Hospital [...] | |||||||||||||
Full Title: Pharmacogenomics of Mood Stabilizer Response in Bipolar Disorder | |||||||||||||
Medical condition: The goal of this work is to identify genes associated with good response of bipolar patients to two commonly used mood stabilizing agents, lithium and valproate. 1. All patients will be started on ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018195-33 | Sponsor Protocol Number: D1443L00079 | Start Date*: 2010-05-11 | |||||||||||
Sponsor Name:Centro de Investigación Biomédica en Red en el Área de Salud Mental (CIBERSAM) | |||||||||||||
Full Title: Eficacia de quetiapina de liberación prolongada vs. placebo como terapia coadyuvante al tratamiento eutimizante en el control de los síntomas subsindrómicos del trastorno bipolar | |||||||||||||
Medical condition: Terapia coadyuvante en el control de los síntomas subsindrómicos del trastorno bipolar | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004746-81 | Sponsor Protocol Number: | Start Date*: 2009-07-20 | ||||||||||||||||
Sponsor Name:Parnassia-BAVO groep [...] | ||||||||||||||||||
Full Title: Effect of amiloride on lithium-induced chronic nephropathy. Comparing discontinuation of lithium treatment to adding amiloride while continuing lithium treatment. | ||||||||||||||||||
Medical condition: Renal failure due to long-term use of lithium salts in patients with bipolar disorders. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004088-26 | Sponsor Protocol Number: A1281201 | Start Date*: 2020-09-03 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: 26-WEEK OPEN-LABEL EXTENSION STUDY EVALUATING THE SAFETY AND TOLERABILITY OF FLEXIBLE DOSES OF ORAL ZIPRASIDONE IN CHILDREN AND ADOLESCENTS WITH BIPOLAR I DISORDER (MOST RECENT EPISODE MANIC) | |||||||||||||
Medical condition: Bipolar Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000370-20 | Sponsor Protocol Number: 2448/2007 | Start Date*: 2008-08-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Evaluation of pharmacokinetic and pharmacodynamic interactions between escitalopram and drugs used for the treatment of bipolar disorders. | |||||||||||||
Medical condition: bipolar disorders | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004872-31 | Sponsor Protocol Number: SCA102833 | Start Date*: 2016-12-21 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: The Evaluation of Lamictal as an Add-on Treatment for Bipolar I Disorder in Children and Adolescents, 10 to 17 Years of Age | |||||||||||||
Medical condition: Bipolar Disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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