- Trials with a EudraCT protocol (92)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
92 result(s) found for: Hallucinations.
Displaying page 1 of 5.
EudraCT Number: 2016-000102-11 | Sponsor Protocol Number: NL55949 | Start Date*: 2016-11-23 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial to evaluate the efficacy of continuous subcutaneous apomorphine infusion in Parkinson’s disease patients with refractory visual hallucinations. | |||||||||||||
Medical condition: Parkinson's disease patients with refractory visual hallucinations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006278-13 | Sponsor Protocol Number: NL24092.042.08 | Start Date*: 2009-02-04 | ||||||||||||||||
Sponsor Name:UMCG | ||||||||||||||||||
Full Title: Motor function optimization in advanced Parkinson’s disease patients, combined with galantamine to prevent visual hallucinations. | ||||||||||||||||||
Medical condition: patients with advanced (>5 years) Parkinson's disease and visual hallucinations. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003962-41 | Sponsor Protocol Number: 17/0909 | Start Date*: 2020-03-23 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Trial of Ondansetron as a Parkinson’s HAllucinations Treatment | |||||||||||||
Medical condition: Adults aged over 18 years with Parkinson's disease and visual hallucinations | |||||||||||||
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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: 2011-001520-37 | Sponsor Protocol Number: KETECT | Start Date*: 2014-02-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Skåne University Hospital, Malmö | |||||||||||||||||||||||||||||||||
Full Title: Ketamine as an alternative to electroconvulsive therapy for treatment of major depressive disorder | |||||||||||||||||||||||||||||||||
Medical condition: Major depression disorder | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001722-25 | Sponsor Protocol Number: ZonMw80-83600-98-10226 | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Cholinesterase inhibitors to slow progression of visual hallucinations in Parkinson’s disease: a multi-center placebo-controlled trial (CHEVAL) | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002227-13 | Sponsor Protocol Number: ACP-103-045 | Start Date*: 2018-02-04 | ||||||||||||||||
Sponsor Name:ACADIA Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A Double-blind, Placebo-controlled, Relapse Prevention Study of Pimavanserin for the Treatment of Hallucinations and Delusions Associated With Dementia-related Psychosis | ||||||||||||||||||
Medical condition: Hallucinations and Delusions Associated With Dementia-related Psychosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) SK (Prematurely Ended) BG (Completed) ES (Prematurely Ended) PL (Prematurely Ended) FR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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: 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: 2010-020008-31 | Sponsor Protocol Number: ACP-103-019 | Start Date*: 2013-10-25 |
Sponsor Name:ACADIA Pharmaceuticals Inc | ||
Full Title: A Single center, Double-Blind, Placebo-Controlled Study to Examine the Safety and Efficacy of Pimavanserin for the Treatment of Psychosis in Alzheimer’s Disease | ||
Medical condition: Psychosis associated with Alzheimer's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000458-23 | Sponsor Protocol Number: 3418363 | Start Date*: 2013-05-07 |
Sponsor Name:Niuvannniemi Hospital | ||
Full Title: Sodium benzoate for treatment of attenuated/transient psychosis. A randomized placebo-controlled trial | ||
Medical condition: attenuated/transient psychosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011799-31 | Sponsor Protocol Number: DIM19 | Start Date*: 2009-10-02 | |||||||||||
Sponsor Name:Medivation, Inc | |||||||||||||
Full Title: CONTACT: A Phase 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled Six-Month Safety and Efficacy Study of Dimebon in Patients with Moderate-to-Severe Alzheimer’s Disease and Neuropsychiat... | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IE (Completed) ES (Completed) PT (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
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: 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: 2005-004109-27 | Sponsor Protocol Number: 2.12.05 | Start Date*: 2006-03-24 |
Sponsor Name:Neuropsychiatric clinic | ||
Full Title: A double-blind, placebo-controlled multi-centre trial of memantine in patients with Parkinsons’ disease dementia or dementia with Lewy bodies | ||
Medical condition: Parkinsons disease (PD)and dementia with Lewy bodies (DLB) are both common disease of the elderly. The majority of patients who survive for more than 10 years with PD eventually develope dementia ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001515-10 | Sponsor Protocol Number: KAR-031 | Start Date*: 2022-12-12 | ||||||||||||||||
Sponsor Name:Karuna Therapeutics | ||||||||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Relapse Prevention Study to Evaluate the Safety and Efficacy of KarXT for the Treatment of Psychosis Associated with Alzheimer’s Disease Deme... | ||||||||||||||||||
Medical condition: Psychosis Associated with Alzheimer’s Disease Dementia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) SK (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) BG (Trial now transitioned) DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003076-39 | Sponsor Protocol Number: P11-05 | Start Date*: 2012-10-10 | |||||||||||
Sponsor Name:Bioprojet | |||||||||||||
Full Title: A randomized, double blind study comparing BF2.649 (Pitolisant) to placebo in two parallel groups on the weekly frequency of cataplexy attacks and Excessive Daytime Sleepiness in narcoleptic patien... | |||||||||||||
Medical condition: Narcolepsy with Cataplexy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001041-15 | Sponsor Protocol Number: N3D/FOR-OCA-06 | Start Date*: 2004-07-26 |
Sponsor Name:Neuro3d | ||
Full Title: MULTICENTRE, DOUBLE-BLIND, RISING DOSE PARALLEL GROUP STUDY OF THE EFFICACY AND TOLERABILITY OF OCAPERIDONE VERSUS OLANZAPINE IN SCHIZOPHRENIC PATIENTS | ||
Medical condition: The populations of the study will be: -schizophrenic patients according to DSM IV-TR diagnosis -have to present the first symptoms of the schizophrenia for at least one year -have to present an exa... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: LV (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002782-37 | Sponsor Protocol Number: ENT05 | Start Date*: 2005-11-17 |
Sponsor Name:Heart of England NHS Foundation Trust | ||
Full Title: A Randomised Trial of Inhaled Entonox Plus Local Anaesthesia Versus Intravenous Midazolam Plus Local Anaesthesia To Improve Pain Control During Bone Marrow Biopsy | ||
Medical condition: This study will involve a group of patients requiring diagnostic bone marrow aspiration and biopsy. The reasons for these will include haematological abnormalities of the blood count , which may be... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016955-23 | Sponsor Protocol Number: ASCOTALCO | Start Date*: 2010-06-25 | |||||||||||
Sponsor Name:AZIENDA USL 2 DI LUCCA | |||||||||||||
Full Title: Assessment of association efficacy of colinergic precursor and cholinesterasic inhibitor somministered transdermal in patient with Alzheimer`s disease and severe behavioural disturbances | |||||||||||||
Medical condition: patient with Alzheimer disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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 |
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