- Trials with a EudraCT protocol (86)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
86 result(s) found for: Schizophrenia and other psychotic disorders.
Displaying page 1 of 5.
| 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: 2019-000470-36 | Sponsor Protocol Number: SEP361-301 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double-blind, Parallel-group, Placebo-controlled, Fixed-dose, Multicenter Study to Evaluate the Efficacy and Safety of SEP-363856 in Acutely Psychotic Subjects with Schizophrenia | ||||||||||||||||||
| Medical condition: Schizophrenia | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BG (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-000709-36 | Sponsor Protocol Number: 15/0947 | Start Date*: 2016-11-23 | ||||||||||||||||||||||||||
| Sponsor Name:UCL | ||||||||||||||||||||||||||||
| Full Title: Research into Antipsychotic Discontinuation and Reduction (RADAR): A Randomised Controlled Trial | ||||||||||||||||||||||||||||
| Medical condition: Schizophrenia, delusional disorders, schizoaffective disorder, psychosis | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2019-000697-37 | Sponsor Protocol Number: SEP361-302 | Start Date*: 2019-09-06 | |||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Randomized, Double-blind, Parallel-group, Placebo-controlled, Fixed-dose, Multicenter Study to Evaluate the Efficacy and Safety of SEP-363856 in Acutely Psychotic Subjects with Schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000240-26 | Sponsor Protocol Number: CBD_ADD_IN | Start Date*: 2013-10-29 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Cannabidiol as an add-on therapy in treatment-refractory psychotic disorders | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002713-35 | Sponsor Protocol Number: AXCT01-01-03-2013 | Start Date*: 2014-07-29 | |||||||||||
| Sponsor Name:MediPsych SA | |||||||||||||
| Full Title: Randomized, controlled trial of the effectiveness of add-on tolcapone to usual antipsychotic therapy on cognitive and negative symptoms of patients with schizophrenia genotyped for COMT polymorphisms | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000053-27 | Sponsor Protocol Number: MELIA | Start Date*: 2020-07-09 |
| Sponsor Name:UMC Utrecht | ||
| Full Title: The MEtformin-LIfestyle in Antipsychotic users trial (MELIA): optimizing the use of metformin in the management of antipsychotic-induced weight gain. | ||
| Medical condition: Antipsychotic-induced weight gain (AiWG) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001555-41 | Sponsor Protocol Number: SEP361-201 | Start Date*: 2016-10-27 | |||||||||||
| Sponsor Name:SUNOVION PHARMACEUTICALS INC. | |||||||||||||
| Full Title: A 4-Week, Randomized, Double-blind, Parallel-group, Placebo-controlled, Flexibly-dosed, Multicenter Study to Evaluate the Efficacy and Safety of SEP-363856 in Acutely Psychotic Adult Subjects With ... | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000581-17 | Sponsor Protocol Number: CVL-231-2002 | Start Date*: 2022-10-18 | ||||||||||||||||
| Sponsor Name:Cerevel Therapeutics, LLC | ||||||||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of Two Fixed Doses (15 mg and 30 mg QD) of CVL-231 in Participants With Schizophreni... | ||||||||||||||||||
| Medical condition: Patients with schizophrenia who are experiencing an acute exacerbation of psychosis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) BG (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-000580-52 | Sponsor Protocol Number: CVL-231-2001 | Start Date*: 2022-11-02 | ||||||||||||||||
| Sponsor Name:Cerevel Therapeutics, LLC | ||||||||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of Two Fixed Doses (10 mg and 30 mg QD) of CVL-231 in Participants With Schizophreni... | ||||||||||||||||||
| Medical condition: Patients with schizophrenia who are experiencing an acute exacerbation of psychosis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BG (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-000696-16 | Sponsor Protocol Number: SEP361-303 | Start Date*: 2019-09-06 | ||||||||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | ||||||||||||||||||
| Full Title: An Open-label Extension Study to Assess the Safety and Tolerability of SEP-363856 in Subjects with Schizophrenia | ||||||||||||||||||
| Medical condition: Schizophrenia | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: LV (Completed) BG (Completed) HR (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-000212-22 | Sponsor Protocol Number: GWAP1241 | Start Date*: 2013-12-13 | |||||||||||
| Sponsor Name:GW Research Ltd | |||||||||||||
| Full Title: A double-blind, randomised, placebo-controlled, parallel group study of GWP42003 as adjunctive therapy in the first line treatment of schizophrenia or related psychotic disorder | |||||||||||||
| Medical condition: Schizophrenia or related psychotic disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) PL (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-016715-38 | Sponsor Protocol Number: TEAprotocolversion3-12102009FINAL | Start Date*: 2010-02-08 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University of Copenhagen | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: The TEA Trial- Tolerance and Effect of Antipsychotics in children and adolescents with psychosis An investigator-initiated, phase IV, randomised double-blind multi-centre trial of the benefits and... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: non-organic and non-drug-induced psychosis, meeting the criteria for ICD-10 diagnoses: F20, F22-F29 and F30.2, F31.2, F31.5, F32.3 and F33.3. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2010-019897-33 | Sponsor Protocol Number: 2522518514 | Start Date*: 2011-04-14 |
| Sponsor Name:erasmus mc | ||
| Full Title: Selective D1 activation by addition of L-Dopa to antipsychotic treatment in patients with schizophrenia | ||
| Medical condition: patients with psychotic symptoms, diagnosed with schizophrenia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004504-35 | Sponsor Protocol Number: RF-2010-2311148 | Start Date*: 2013-02-26 | |||||||||||
| Sponsor Name:IRCCS CENTRO SAN GIOVANNI DI DIO FATEBENEFRATELLI | |||||||||||||
| Full Title: The use of Oxytocin as adjunctive therapy for the treatment of schizophrenia: a randomized, double blind trial | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001278-44 | Sponsor Protocol Number: CLZ_TRS_TEA | Start Date*: 2021-05-26 |
| Sponsor Name:Fundación Hospital Provincial de Castellón | ||
| Full Title: Comparative analysis of the effectiveness of clozapine in resistant schizophrenia and schizoafective disorder. | ||
| Medical condition: Treatment-resistant schizophrenia and schizoafective disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-006151-20 | Sponsor Protocol Number: D1449L00029 | Start Date*: 2006-08-29 | |||||||||||
| Sponsor Name:University of Erlangen-Nuremberg | |||||||||||||
| Full Title: Quetiapine and the dopaminergic epigenetic control – a pilot study | |||||||||||||
| Medical condition: Patients suffering from schizophrenia (ICD10: F20.x) Healthy controls | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002176-83 | Sponsor Protocol Number: SNP-S-01 | Start Date*: 2015-04-01 | |||||||||||
| Sponsor Name:Clinirx Tangent Research | |||||||||||||
| Full Title: A randomized trial administering Sodium Nitroprusside vs. placebo as add-on to antipsychotics in patients with schizophrenia | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: RO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001337-40 | Sponsor Protocol Number: BXCL501-105 | Start Date*: 2021-10-05 | |||||||||||||||||||||
| Sponsor Name:BioXcel Therapeutics, Inc. | |||||||||||||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DETERMINE EFFICACY AND SAFETY OF BXCL501 IN AGITATION ASSOCIATED WITH PEDIATRIC SCHIZOPHRENIA AND BIPOLAR DISORDER | |||||||||||||||||||||||
| Medical condition: Subject that meets DSM-5 criteria for schizophrenia, schizoaffective, or schizophreniform disorder, or other specified/unspecified schizophrenia spectrum and/or other psychotic disorders OR Subjec... | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Restarted) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
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