- Trials with a EudraCT protocol (97)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
97 result(s) found for: Mania.
Displaying page 1 of 5.
EudraCT Number: 2008-000281-23 | Sponsor Protocol Number: Oxford University(None) | Start Date*: 2009-09-10 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: Melatonin in Acute Mania Investigation (MIAMI-UK) | ||||||||||||||||||
Medical condition: Bipolar Disorder (mania and hypomania) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023992-24 | Sponsor Protocol Number: MEMAP1 | Start Date*: 2011-08-26 | |||||||||||
Sponsor Name:University of Leipzig | |||||||||||||
Full Title: International randomised double-blind placebo-controlled study on the initial treatment of acute mania with methylphenidate | |||||||||||||
Medical condition: acute mania and hypomania (ICD-10: F30.0, F30.1, F31.0, F31.1) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) BE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000323-86 | Sponsor Protocol Number: N/A | Start Date*: 2017-05-05 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: A randomised, parallel group, double blind, placebo controlled, add on clinical trial to investigate whether the lithium mimetic, ebselen, can reduce symptoms of hypomania and mania in bipolar pati... | ||||||||||||||||||
Medical condition: Patients with bipolar disorder meeting DSM-5 criteria for hypomania or mania | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005959-42 | Sponsor Protocol Number: CN138-502 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||
Full Title: A 12-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study To Evaluate the Efficacy and Safety of Adjunctive Aripiprazole Therapy in the Treatment of Mania in Bipolar I Disorder Pat... | |||||||||||||
Medical condition: Bipolar I Mania (manic or mixed episode) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) CZ (Completed) AT (Completed) HU (Completed) IT (Completed) PL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001482-17 | Sponsor Protocol Number: F1D-MC-HGKQ(b) | Start Date*: 2004-10-15 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: Olanzapine Versus Divalproex and Placebo in the Treatment of Mild to Moderate Mania Associated with Bipolar I disorder. | ||
Medical condition: Manic or Mixed Episodes Associated with Bipolar I Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: LT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-007190-20 | Sponsor Protocol Number: D144AC00003 | Start Date*: 2009-12-14 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: 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) i... | |||||||||||||
Medical condition: Acut mania in subjects with bipolar I disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018409-13 | Sponsor Protocol Number: P05691 | Start Date*: 2012-08-23 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering | |||||||||||||
Full Title: A Phase 3b, Multicenter, Double-Blind, Fixed-Dose, Parallel-Group, Three Week Placebo Controlled Trial Evaluating the Safety and Efficacy of Asenapine in Subjects With Bipolar 1 Disorder Experie... | |||||||||||||
Medical condition: Bipolar 1 Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006426-26 | Sponsor Protocol Number: D1443L00009 | Start Date*: 2007-01-17 |
Sponsor Name:AstraZeneca AB | ||
Full Title: FAST – A randomised, open-label, parallel, multicentre Phase IIIb Study to evaluate the Efficacy and Safety of Quetiapine IR titrared over 4 Days in Patients with Acute Psychosis (Rapid versus Conv... | ||
Medical condition: Patients requiring treatment, as judged by the Investigator, for an acute episode of schizophrenia, schizoaffective disorder, psychosis NOS or bipolar mania (according to DSM-IV criteria). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-005072-32 | Sponsor Protocol Number: R&D2004/39 | Start Date*: 2005-12-19 |
Sponsor Name:Kings College London (IOP) / South London and Maudsley NHS Trust (Co-sponsorship) | ||
Full Title: Is it possible to modify the course of manic relapse? A pilot study of the effectiveness of quetiapine in preventing the development of manic episodes in Bipolar Disorder. | ||
Medical condition: Bipolar Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002133-13 | Sponsor Protocol Number: PRA/BIA-2093-204 | Start Date*: 2005-10-21 |
Sponsor Name:BIAL - Portela & Ca, S.A. | ||
Full Title: EFFICACY AND SAFETY OF ESLICARBAZEPINE ACETATE (BIA 2-093) IN ACUTE MANIC EPISODES ASSOCIATED WITH BIPOLAR I DISORDER IN A DOUBLE-BLIND, FIXED MULTIPLE DOSE, RANDOMIZED, PLACEBO-CONTROLLED, MULTICE... | ||
Medical condition: Patients with acute manic episodes fulfilling DSM-IV criteria for Bipolar I Disorder. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-005010-37 | Sponsor Protocol Number: 62 | Start Date*: 2005-08-16 |
Sponsor Name:Suffolk Mental Health Partnerships Trust | ||
Full Title: Enhancing cognition in bipolar disorder | ||
Medical condition: Bipolar affective disorder, currently in remission | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002222-20 | Sponsor Protocol Number: 331-201-00080 | Start Date*: 2018-02-23 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind Trial of Brexpiprazole versus Placebo for the Acute Treatment of Manic Episodes, With or Without Mixed Features, Associated With Bipolar I Disorder | |||||||||||||
Medical condition: Treatment of Manic Episodes Associated with Bipolar I Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002190-20 | Sponsor Protocol Number: 331-201-00081 | Start Date*: 2018-04-09 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind Trial of Brexpiprazole versus Placebo for the Acute Treatment of Manic Episodes, With or Without Mixed Features, Associated With Bipolar I Disorder | |||||||||||||
Medical condition: Treatment of Manic Episodes Associated with Bipolar I Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000589-11 | Sponsor Protocol Number: F1D-MC-HGKR | Start Date*: 2004-08-10 |
Sponsor Name:ELI LILLY and COMPANY | ||
Full Title: Protocol F1D-MC-HGKR. Olanzapine Plus Carbamazepine Versus Carbamazepine Alone in the Treatment of Manic or Mixed Episodes Associated with Bipolar I Disorder | ||
Medical condition: Manic or Mixed Episodes Associated with Bipolar I Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000405-83 | Sponsor Protocol Number: VP-VYV-683-3201 | Start Date*: 2021-04-09 | |||||||||||
Sponsor Name:Vanda Pharmaceuticals Inc. | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of iloperidone for 4 weeks in the treatment of patients with acute manic episodes associated wi... | |||||||||||||
Medical condition: Acute manic episodes associated with Bipolar I Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003705-17 | Sponsor Protocol Number: LUMC-NECH-201801-ACA | Start Date*: 2019-03-22 |
Sponsor Name:LUMC | ||
Full Title: Prevention of neuropsychiatric adverse effects caused by dexamethasone: translational insights from a placebo-controlled trial with hydrocortisone. | ||
Medical condition: Neuropsychiatric adverse effects which can be caused by dexamethasone. For example delirium, anxiety, depression, mania and psychosis. But also cognitive impairment and sleep disturbance. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000113-18 | Sponsor Protocol Number: CLIC477D2302 | Start Date*: 2004-09-23 |
Sponsor Name:Novartis Farmacéutica, S.A. | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy, safety and tolerability of licarbazepine 750-2500 mg/d combined with risperidone in the treatment of mani... | ||
Medical condition: Bipolar I disorder, manic and mixed episodes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) HU (Completed) FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-006706-69 | Sponsor Protocol Number: DUAG9V1.03_10.06.2022 | Start Date*: 2022-06-22 | |||||||||||
Sponsor Name:Psychiatry – Aalborg University Hospital, Unit for Psychiatric Research | |||||||||||||
Full Title: Lithium versus cariprazine in the acute phase treatment of bipolar depression: a pragmatic head-to-head open, randomized multicenter study. The 9th study of the Danish University Antidepressant Gro... | |||||||||||||
Medical condition: Bipolar disorder, current depressive episode. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007483-42 | Sponsor Protocol Number: D1050256 | Start Date*: 2009-10-21 | |||||||||||
Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
Full Title: A 24-Week, Flexible-Dose, Open-label Extension Study of Lurasidone for the Treatment of Bipolar I Depression | |||||||||||||
Medical condition: Bipolar I depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) FR (Completed) SK (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004357-94 | Sponsor Protocol Number: NPS-2005-1 | Start Date*: 2006-01-20 |
Sponsor Name:Nordfjord Psychiatric Centre | ||
Full Title: Escitalopram in bipolar depression: a placebo-controlled study of acute and maintenance treatment. | ||
Medical condition: Patients with bipolar disorder in a depressive episode are randomised to receive escitalopram or placebo for eight weeks. Responders to escitalopram are re-randomised to placebo or escitalopram for... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
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