- Trials with a EudraCT protocol (56)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
56 result(s) found for: Young Mania Rating Scale.
Displaying page 1 of 3.
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: 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: 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: 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: 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: 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: 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: 2007-006561-32 | Sponsor Protocol Number: OxyCog-01 | Start Date*: 2009-11-05 |
Sponsor Name:LWL University Hospital Bochum | ||
Full Title: Effects of intranasal application of oxytocin on empathy and mentalising in patients with psychotic disorders and severe personality disorders | ||
Medical condition: Schizophrenia, bipolar disorder, major depression, personality disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000606-20 | Sponsor Protocol Number: A1281132 | Start Date*: 2015-04-03 |
Sponsor Name:Pfizer, Inc. | ||
Full Title: Four Week, Double-Blind, Placebo Controlled Phase III Trial Evaluating The Efficacy, Safety And Pharmacokinetics Of Flexible Doses Of Oral Ziprasidone In Children And Adolescents With Bipolar I Dis... | ||
Medical condition: Bipolar Disorder | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2004-001308-11 | Sponsor Protocol Number: F1D-XM-HGLW | Start Date*: 2004-08-19 | |||||||||||
Sponsor Name:Lilly.S.A. | |||||||||||||
Full Title: Optimal Treatment Duration with Olanzapine following Remission of Manic or Mixed Episode. An Open-Label, Randomized Trial Comparing Two Treatment Strategies | |||||||||||||
Medical condition: to compare the efficacy in the prevention of relapse to manic, depressive, or mixed episodes in two groups of bipolar I patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 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: 2007-001541-18 | Sponsor Protocol Number: T3RIS22007 | Start Date*: 2007-10-08 | |||||||||||
Sponsor Name:Institute of Psychophysiology and Rehabilitation (IRP) of the Kaunas University of Medicine | |||||||||||||
Full Title: Triiodothyronine as an adjunct in treatment of acute schizophrenia | |||||||||||||
Medical condition: Acute Schizoprenia episode | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000114-40 | Sponsor Protocol Number: CLIC477D2303 | Start Date*: 2004-11-19 |
Sponsor Name:Novartis Pharma AG | ||
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 lithium or valproate in the treatmen... | ||
Medical condition: Bipolar I disorder, manic and mixed episodes DSM-IV criteria 296.0, 296.4 or 296.6 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) SK (Prematurely Ended) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-022647-38 | Sponsor Protocol Number: P06107 | Start Date*: 2011-11-16 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation | |||||||||||||
Full Title: Efficacy and Safety of 3-Week Fixed-Dose Asenapine Treatment in Pediatric Acute Manic or Mixed Episodes Associated with Bipolar I Disorder (Protocol No. P06107) | |||||||||||||
Medical condition: Acute Manic or Mixed Episodes Associated with Bipolar I Disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003002-12 | Sponsor Protocol Number: CMIJ821X2201 | Start Date*: 2019-04-08 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A multi-center, randomized, subject and investigator-blinded, placebo-controlled, active comparator, parallel-group proof of concept study to evaluate the efficacy, safety, tolerability, and pharma... | |||||||||||||
Medical condition: Treatment Resistant Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006861-39 | Sponsor Protocol Number: GH001-BD-202 | Start Date*: 2022-06-20 | |||||||||||
Sponsor Name:GH Research Ireland Limited | |||||||||||||
Full Title: A Phase 2 Clinical Trial of GH001 in Patients with Bipolar II Disorder and a Current Major Depressive Episode (GH001-BD-202) | |||||||||||||
Medical condition: Bipolar II Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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