- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
67 result(s) found for: Aggression.
Displaying page 1 of 4.
| EudraCT Number: 2012-004299-20 | Sponsor Protocol Number: ELND005-AG201 | Start Date*: 2013-04-25 |
| Sponsor Name:Transition Therapeutics Ireland Ltd | ||
| Full Title: A Prospective, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Efficacy and Safety Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheime... | ||
| Medical condition: Agitation and Aggression in Moderate to Severe Alzheimer’s Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-005524-15 | Sponsor Protocol Number: ELND005-AG251 | Start Date*: 2013-09-03 |
| Sponsor Name:Elan Pharma International Ltd | ||
| Full Title: A 36-Week Safety Extension Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheimer's Disease. | ||
| Medical condition: Agitation and Aggression in Moderate to severe Alzheimer's Disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000641-23 | Sponsor Protocol Number: CNWL/MC/AFT/01 | Start Date*: 2015-11-24 |
| Sponsor Name:Central and North West London NHS Foundation Trust | ||
| Full Title: Aggression Following TBI: Effectiveness of Risperidone (AFTER)-a feasibility RCT. | ||
| Medical condition: aggression and agitation following on from a traumatic brain injury | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000584-42 | Sponsor Protocol Number: FH1/08 | Start Date*: 2008-08-06 | |||||||||||
| Sponsor Name:Universität Rostock, für diese handelnd Universitätsklinikum | |||||||||||||
| Full Title: Effekte von Zuclopenthixol auf aggressives Verhalten bei Kindern und Jugendlichen mit einer geistigen oder Lernbehinderung (unterdurchschnittlichen Intelligenz) | |||||||||||||
| Medical condition: Aggressive Verhaltensstörungen bei intelligenzgeminderten Kindern und Jugendlichen | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-015629-35 | Sponsor Protocol Number: R076477SCH3038 | Start Date*: 2009-11-05 |
| Sponsor Name:Janssen-Cilag NV/SA | ||
| Full Title: Open-label, single arm, interventional study to explore the efficacy and safety of paliperidone ER in the management of patients with acute agitation and/or aggression | ||
| Medical condition: Subject presenting with acute agitation and/or agression in the context of psychosis, suspected schizophrenia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002140-88 | Sponsor Protocol Number: CL04-ORY-2001 | Start Date*: 2018-09-06 | |||||||||||
| Sponsor Name:Oryzon Genomics S.A. | |||||||||||||
| Full Title: An unicenter, open-label, 1-arm, 8-week study to evaluate the efficacy, safety and tolerability of ORY-2001 in aggression in adult population with Alzheimer’s Disease (AD), Lewy Body Dementia (LBD)... | |||||||||||||
| Medical condition: Agression | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001436-54 | Sponsor Protocol Number: CL06-ORY-2001 | Start Date*: 2019-06-05 | |||||||||||
| Sponsor Name:Oryzon Genomics S. A. | |||||||||||||
| Full Title: A single-center, open-label, single-arm, 13-week study to evaluate the efficacy, safety and tolerability of ORY-2001 in aggression in Alzheimer’s Disease (AD) – REIMAGINE-AD | |||||||||||||
| Medical condition: Aggression in Alzheimer’s Disease (AD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001916-37 | Sponsor Protocol Number: MATRICS_WP6-1 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:RADBOUD UNIVERSITY MEDICAL CENTER | |||||||||||||
| Full Title: The neuropsychological characterization of aggressive behaviour in children and adolescents with Conduct Disorder or Oppositional Defiant Disorder (CD/ODD) | |||||||||||||
| Medical condition: Aggressive behavior in children and adolescents with Conduct Disorder (CD) or Oppositional Defiant Disorder (ODD) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001910-40 | Sponsor Protocol Number: 0305070107 | Start Date*: 2020-06-09 |
| Sponsor Name:Radboud University | ||
| Full Title: Combining emotion recognition training with oxytocin administration: A psychobiological approach | ||
| Medical condition: We examine whether oxytocin administration can improve the effectiveness of emotion recognition training compared to placebo in residential youth with antisocial behavior | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-000389-12 | Sponsor Protocol Number: 3.0 | Start Date*: 2013-09-11 |
| Sponsor Name:Cardiff University | ||
| Full Title: ANti-psychotic Drug REduction in primary care for Adults with Learning Disabilities (ANDREA-LD): A Randomised Double-blind Placebo Controlled Trial | ||
| Medical condition: Aggression and challenging behaviour in adults with learning disabilities | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001127-32 | Sponsor Protocol Number: ACP-103-032 | Start Date*: 2016-09-19 | |||||||||||
| Sponsor Name:ACADIA Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Double-Blind, Placebo-Controlled Study to Examine the Safety and Efficacy of Pimavanserin for the Treatment of Agitation and Aggression in Alzheimer’s Disease | |||||||||||||
| Medical condition: Agitation and Aggression in Alzheimer’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000217-30 | Sponsor Protocol Number: 3098012 | Start Date*: 2015-06-16 | |||||||||||
| Sponsor Name:Orion Corporation | |||||||||||||
| Full Title: EFFICACY OF ORM-12741 ON AGITATION/AGGRESSION SYMPTOMS IN PATIENTS WITH ALZHEIMER’S DISEASE: A RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTICENTRE STUDY OF 12 WEEKS | |||||||||||||
| Medical condition: The agitation/aggression symptoms in patients with Alzheimer’s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) FI (Completed) PL (Completed) BG (Completed) RO (Suspended by CA) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005938-15 | Sponsor Protocol Number: CloTASH-2021-2Version15.10.21 | Start Date*: 2021-11-03 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Health risks and treatment of anabolic-androgenic steroid (AAS) induced hypogonadism among men – a pilot study exploring off-label use of clomiphene citrate to reduce symptoms of androgen deficienc... | ||
| Medical condition: Anabolic androgenic steroid induced hypogonadism among men | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001217-25 | Sponsor Protocol Number: 2016-001217-25 | Start Date*: 2016-09-07 |
| Sponsor Name:Uppsala University | ||
| Full Title: Emotion, Serotonin and Premenstrual Dysphoric Disorder (EmSeP) | ||
| Medical condition: Premenstrual Dysphoric Disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001128-78 | Sponsor Protocol Number: ACP-103-033 | Start Date*: 2017-03-21 | |||||||||||
| Sponsor Name:ACADIA Pharmaceuticals Inc. | |||||||||||||
| Full Title: A 52-Week Open-Label Extension Study of Pimavanserin for the Treatment of Agitation and Aggression in Subjects with Alzheimer’s Disease | |||||||||||||
| Medical condition: Agitation and Aggression in Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000860-10 | Sponsor Protocol Number: 10729 | Start Date*: 2006-06-30 |
| Sponsor Name:H. Lundbeck A/S | ||
| Full Title: An Open-Label Study Investigating the Specific Effects of Memantine in Institutionalised Patients with Alzheimer’s Disease | ||
| Medical condition: Effects of memantine treatment in institutionalised patients with Alzheimer's Disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) BE (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001056-17 | Sponsor Protocol Number: 3606 | Start Date*: 2020-08-14 | ||||||||||||||||
| Sponsor Name:Kings's College London [...] | ||||||||||||||||||
| Full Title: A randomised feasibility trial investigating Sativex® for the treatment of the Agitation & Aggression (A/A) in Alzheimer’s Dementia. | ||||||||||||||||||
| Medical condition: Clinically significant agitation in Alzheimer's Diseases | ||||||||||||||||||
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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: 2008-000243-33 | Sponsor Protocol Number: FARM68SY5C | Start Date*: 2008-09-24 | |||||||||||
| Sponsor Name:ISTITUTO SUPERIORE DI SANITA' | |||||||||||||
| Full Title: Alzheimer disease and antipsycotics: a long term multicenter randomized clinical trial | |||||||||||||
| Medical condition: BPSD in Alzheimer disease | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002471-18 | Sponsor Protocol Number: | Start Date*: 2019-01-18 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: The clinical effectiveness and cost effectiveness of clozapine for inpatients with borderline personality disorder: randomised controlled trial | |||||||||||||
| Medical condition: Borderline Personality Disorder | |||||||||||||
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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: 2012-000517-37 | Sponsor Protocol Number: CIAOProject | Start Date*: 2012-11-08 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: A pilot study of Concerta XL in adult offenders with ADHD | |||||||||||||
| Medical condition: Attention deficit hyperactivity disorder (ADHD) | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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