- Trials with a EudraCT protocol (41)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    41 result(s) found for: Verbal fluency test.
                    
                
			
   			
		
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	| EudraCT Number: 2011-005476-41 | Sponsor Protocol Number: MMHSCT1096 | Start Date*: 2012-05-18 | |||||||||||
| Sponsor Name:Manchester Mental Health and Social Care Trust | |||||||||||||
| Full Title: Ketamine augmentation of ECT to improve outcomes in depression | |||||||||||||
| Medical condition: Depressive disorder requiring treatment with electroconvulsive treatment (ECT) | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004297-34 | Sponsor Protocol Number: 236252 | Start Date*: 2018-03-31 | |||||||||||
| Sponsor Name:Aston University | |||||||||||||
| Full Title: A placebo controlled double blind randomised controlled proof of concept study of zolpidem for the treatment of motor and cognitive deficits in late-stage Parkinson’s | |||||||||||||
| Medical condition: Parkinson's Disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003945-10 | Sponsor Protocol Number: 01-APN-08 | Start Date*: 2009-01-20 | 
| Sponsor Name:Centre hospitalier universitaire de nice | ||
| Full Title: ACTION OF THE AMANTADINE ON POST STROKE APHASIC PATIENTS LANGUAGE AND COMMUNICATION | ||
| Medical condition: post stroke chronic aphasia patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001850-13 | Sponsor Protocol Number: GLP-1/MCI | Start Date*: 2015-09-11 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA DI PARMA | |||||||||||||
| Full Title: Long-acting exenatide: a tool to stop cognitive decline in patients with mild cognitive impairment with or without dysglycemia? | |||||||||||||
| Medical condition: Moderate cognitive impairment | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-003410-15 | Sponsor Protocol Number: 6251 7976 | Start Date*: 2005-11-21 | 
| Sponsor Name:Neurology Unit | ||
| Full Title: A twelve-month double-blind placebo-controlled cross-over study of the effect ofAricept treatment on cognitive dysfunction in multiple sclerosis. | ||
| Medical condition: Multiple sclerosis is a devastating inflammation in the central nervous system and it can often give cognitive dysfunction, affecting memory, mental concentration. Lately it has been shown that the... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002326-36 | Sponsor Protocol Number: 2016-858 | Start Date*: 2016-11-09 | ||||||||||||||||
| Sponsor Name:Region Hovedstadens psykiatriske hospital | ||||||||||||||||||
| Full Title: Effects of erythropoietin (EPO) on cognitive side-effects of electroconvulsive therapy (ECT) (EPO-T) | ||||||||||||||||||
| Medical condition: Unipolar/bipolar depression | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-000618-32 | Sponsor Protocol Number: GNC-501 | Start Date*: 2022-09-29 | ||||||||||||||||
| Sponsor Name:GENEURO SA | ||||||||||||||||||
| Full Title: Temelimab as a Disease Modifying Therapy in Patients with Neurological, Neuropsychological, and Psychiatric (=Neuropsychiatric) Symptoms in Post-COVID-19 or Postacute Sequelae of COVID-19 (PASC) Sy... | ||||||||||||||||||
| Medical condition: Postacute Sequelae of COVID-19 (PASC) Syndrome | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2004-005078-22 | Sponsor Protocol Number: QUETIAPINKOGNSCHIZOPHR | Start Date*: 2005-04-18 | 
| Sponsor Name:Medical School of Hannover | ||
| Full Title: Quetiapin: Zur Sicherheit, Verträglichkeit und zum Einfluss auf kognitive Funktionen bei Patienten/innen mit einer schizophrenen Psychose Quetiapine: safety and influence on cognitive functions i... | ||
| Medical condition: Patients with schizophrenia, who are not in an acute state of psychosis at enrolment (PANSS score < 80) and who do not show criteria of moderate depression, but may show depression-like symptoms co... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-000903-17 | Sponsor Protocol Number: CN138-166 | Start Date*: 2005-02-23 | 
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||
| Full Title: A Prospective, Multicenter, Open-Label Study to Evaluate the Effectiveness and the Effect on Cognitive Functioning of a Treatment with Aripiprazole in a Broad Range of Schizophrenic Patients | ||
| Medical condition: Schizophrenia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004023-24 | Sponsor Protocol Number: PRETEC-EPO | Start Date*: 2016-12-15 | ||||||||||||||||
| Sponsor Name:Copenhagen Affective Disorder research Center (CADIC), Psychiatric Centre Copenhagen, Rigshospitalet | ||||||||||||||||||
| Full Title: Effect of erythropoietin (EPO) on cognitive function and frontal lobe activity in patients with bipolar disorder and unipolar depression in remission (PRETEC-EPO) | ||||||||||||||||||
| Medical condition: Bipolar disorder and unipolar depression | ||||||||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2005-002038-36 | Sponsor Protocol Number: 11018 | Start Date*: 2007-02-27 | |||||||||||
| Sponsor Name:H. Lundbeck A/S | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, 6-month study of the efficacy and safety of memantine in patients with Parkinson’s disease dementia or dementia with Lewy Bodies | |||||||||||||
| Medical condition: Patients with Parkinson’s disease dementia or dementia with Lewy Bodies | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) GB (Completed) AT (Completed) IT (Completed) DE (Completed) FR (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000630-30 | Sponsor Protocol Number: AC-AD-003 | Start Date*: 2015-11-26 | 
| Sponsor Name:AXON NEUROSCIENCE SE | ||
| Full Title: “ADAMANT” A 24-months randomised, placebo-controlled, parallel group, double blinded, multi centre, phase 2 study to assess safety and efficacy of AADvac1 applied to patients with mild Alzheimer’s ... | ||
| Medical condition: Alzheimer’s disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) CZ (Completed) SE (Completed) DE (Completed) SK (Completed) SI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-004498-18 | Sponsor Protocol Number: HUB-NEU-2019-01 | Start Date*: 2020-06-30 | |||||||||||
| Sponsor Name:Dr. Jordi Gascón / Dra. Lola Ledesma | |||||||||||||
| Full Title: EFFICACY AND SAFETY CLINICAL TRIAL WITH EFAVIRENZ IN PATIENTS DIAGNOSED WITH ADULT NIEMANN-PICK TYPE C WITH COGNITIVE IMPAIRMENT | |||||||||||||
| Medical condition: Niemann Pick tipo C (NPC) | |||||||||||||
					
						
							
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003473-94 | Sponsor Protocol Number: UCL-2016-121 | Start Date*: 2019-05-20 | 
| Sponsor Name:Cliniques Universitaires Saint-Luc | ||
| Full Title: Tau and Amyloid PET imaging in normal aging, early Alzheimer's disease and related syndroms. | ||
| Medical condition: Alzheimer’s disease (AD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002631-17 | Sponsor Protocol Number: IIBSP-DUO-2015-46 | Start Date*: 2015-11-19 | 
| Sponsor Name:Institut de Recerca del Hospital de la Santa Creu i Sant Pau | ||
| Full Title: An intra-subject, randomized, double blind, crossover study comparing immediate-release oral LD (IR-LD) and L-dopa/carbidopa intestinal gel (LCIG) over cognition and mood in non-demented advanced P... | ||
| Medical condition: Parkinson disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004537-16 | Sponsor Protocol Number: 29BRC19.0280 | Start Date*: 2020-03-26 | |||||||||||
| Sponsor Name:CHRU de Brest | |||||||||||||
| Full Title: Comparison of an inhaled sedation strategy to an intravenous sedation strategy in ICU patients treated with invasive mechanical ventilation | |||||||||||||
| Medical condition: Prevention of delirium | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003053-25 | Sponsor Protocol Number: 1466 | Start Date*: 2012-06-18 | |||||||||||
| Sponsor Name:Research and Enterprise Department | |||||||||||||
| Full Title: A randomised, double blind, placebo controlled trial to evaluate the effect of Rivastigmine on gait in people with Parkinson’s disease who have fallen. | |||||||||||||
| Medical condition: Parkinson's disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011594-33 | Sponsor Protocol Number: SMRI-07TGF-1152 | Start Date*: 2009-11-02 | |||||||||||
| Sponsor Name:LWL University Hospital Bochum, Ruhr-University Bochum | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled study of tetrabenazine as adjunctive therapy to risperidone in first-episode schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003284-19 | Sponsor Protocol Number: CTU/2013/073 | Start Date*: 2017-01-24 | 
| Sponsor Name:University College London | ||
| Full Title: DEpletion of Serum amyloid P component In Alzheimer’s Disease: DESPIAD. Double-blind placebo controlled randomised phase IIb trial of SAP depletion by CPHPC in mild Alzheimer’s disease. | ||
| Medical condition: Alzheimer's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000766-42 | Sponsor Protocol Number: WN42171 | Start Date*: 2020-07-23 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: AN OPEN-LABEL, MULTICENTER, ROLLOVER STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND EFFICACY OF LONG-TERM GANTENERUMAB ADMINISTRATION IN PARTICIPANTS WITH ALZHEIMER'S DISEASE | ||||||||||||||||||
| Medical condition: Alzheimer's Disease | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) PT (Prematurely Ended) PL (Prematurely Ended) HU (Completed) DE (Completed) FR (Completed) IT (Prematurely Ended) LT (Completed) NL (Completed) BE (Completed) FI (Completed) HR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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