- Trials with a EudraCT protocol (357)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
357 result(s) found for: Cognitive control.
Displaying page 1 of 18.
EudraCT Number: 2016-001248-20 | Sponsor Protocol Number: COG-PRO | Start Date*: 2016-07-20 |
Sponsor Name:Centre François Baclesse | ||
Full Title: Impact of new generation hormono-therapy on cognitive functions in elderly patients treated for a metastatic prostate cancer | ||
Medical condition: Metastatic prostate cancer | ||
Disease: | ||
Population Age: Elderly | Gender: Male | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003331-10 | Sponsor Protocol Number: HC03 | Start Date*: 2017-10-16 |
Sponsor Name:Leiden University | ||
Full Title: Acute effects of 40 mg cortisol on emotion and cognition. | ||
Medical condition: None. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000504-37 | Sponsor Protocol Number: 2020PI215 | Start Date*: 2021-04-01 | ||||||||||||||||
Sponsor Name:CHRU DE NANCY | ||||||||||||||||||
Full Title: Characterization by PET-CT with 18F-FDG of brain lesions in young subjects with sequential psycho-cognitive disorders following severe COVID19 | ||||||||||||||||||
Medical condition: young subjects with sequential psycho-cognitive disorders in the aftermath of severe COVID-19 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000342-19 | Sponsor Protocol Number: IIT-2017/02 | Start Date*: 2018-10-18 |
Sponsor Name:Otto-von-Guericke-Universität Magdeburg, Medizinische Fakultät | ||
Full Title: Prospective, randomized, double-blind clinical trial phase II for the anti-inflammatory effects of Curazink (zinc histidine) for 8 weeks in elderly patients with mild cognitive impairment in Alzhei... | ||
Medical condition: Included are patients with the presence of a moderate or pronounced zinc deficienc and the diagnosis of a mild cognitive disorder, which may be due to an additional investigation (amyloid PET and /... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020724-21 | Sponsor Protocol Number: ADR16SUS2 | Start Date*: 2011-04-06 |
Sponsor Name:Universitätsklinik für Neurologie, Medizinische Universität Wien | ||
Full Title: Amyloid Imaging with [11C]PIB PET and MRI in MCI – a pilot study | ||
Medical condition: Patients with Mild Cognitive Impairment (MCI) will be investigated with PIB PET to determin amyloid pathology | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001846-42 | Sponsor Protocol Number: CAQW051A2104 | Start Date*: 2007-10-05 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A 4-week, parallel-group, randomized, double-blind, placebo-controlled, adaptive proof of concept study of AQW051 at up to three dose levels for the treatment of patients with findings consistent w... | ||||||||||||||||||
Medical condition: Mild Alzheimer’s disease (AD) and amnestic mild cognitive impairment (amnestic MCI) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003891-11 | Sponsor Protocol Number: LMT-01-02-18 | Start Date*: 2019-07-16 | |||||||||||
Sponsor Name:Life Molecular Imaging SA | |||||||||||||
Full Title: An Open Label, Single Center Study, to evaluate the Safety and Imaging Characteristics of [18F]PI-2620 as PET Radioligand for Imaging Tau deposition in the brains of subjects with amnestic mild cog... | |||||||||||||
Medical condition: Alzheimer's Disease Amnestic Mild Cognitive Impairment | |||||||||||||
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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: 2011-001756-12 | Sponsor Protocol Number: UCL-2010-412 | Start Date*: 2012-04-27 |
Sponsor Name:Cliniques Universitaires Saint Luc - UCL | ||
Full Title: Surrogate markers evaluation in pre-demented Alzheimer’s disease patients and healthy elderly controls | ||
Medical condition: Healthy volunteers and Mild Cognitive Impaired patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003209-92 | Sponsor Protocol Number: EVP-6124-016 | Start Date*: 2013-10-22 | ||||||||||||||||
Sponsor Name:Forum Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel, 26 Week, Phase 3 Study of 2 Doses of an Alpha-7 Nicotinic Acetylcholine Receptor Agonist (EVP-6124) or Placebo as an Adjunctive Pro-cogniti... | ||||||||||||||||||
Medical condition: Cognitive impairment associated with schizophrenia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IT (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003208-10 | Sponsor Protocol Number: EVP-6124-015 | Start Date*: 2013-06-28 | ||||||||||||||||
Sponsor Name:Forum Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel, 26 Week, Phase 3 Study of 2 Doses of an Alpha-7 Nicotinic Acetylcholine Receptor Agonist (EVP-6124) or Placebo as an Adjunctive Pro-cogniti... | ||||||||||||||||||
Medical condition: Cognitive impairment associated with schizophrenia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002925-30 | Sponsor Protocol Number: AGO/2012/003 | Start Date*: 2012-09-21 |
Sponsor Name:University Ghent | ||
Full Title: The influence of oxytocin on automatic imitation | ||
Medical condition: Investigate the influence of oxytocin on automatic imitation | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004169-34 | Sponsor Protocol Number: UoB1407 | Start Date*: 2012-02-07 |
Sponsor Name:University of Bristol | ||
Full Title: Effects of Varenicline and Cognitive Bias Modification on Neural Response to Smoking Cues | ||
Medical condition: Healthy volunteer trial: Neural responses to smoking cues Intended indication (Smoking cessation) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000679-25 | Sponsor Protocol Number: IIBSP-CAN-2016-16 | Start Date*: 2016-05-31 |
Sponsor Name:INSTITUT DE RECERCA HSCSP | ||
Full Title: A prospective, randomized, double-blind and placebo-controlled, parallel group, phase II study to compare the efficacy and safety of candesartan versus placebo on cognitive impairment associated wi... | ||
Medical condition: Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003796-17 | Sponsor Protocol Number: CST103/CST139-CLIN-010 | Start Date*: 2020-10-22 | ||||||||||||||||
Sponsor Name:CuraSen Therapeutics, Inc. | ||||||||||||||||||
Full Title: An Open-Label Brain Imaging and Cognition Study to Determine Changes in Cerebral Perfusion and Cognition After Oral Administration of CST-103 or CST-139 | ||||||||||||||||||
Medical condition: Patients with Mild Cognitive Impairment or Parkinson’s Disease | ||||||||||||||||||
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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: 2011-001839-23 | Sponsor Protocol Number: 14137A | Start Date*: 2012-05-14 |
Sponsor Name:H. Lundbeck A/S | ||
Full Title: Interventional randomised, double-blind, parallel-group, placebo-controlled, exploratory study investigating the effects of Lu AA21004 on cognition and BOLD fMRI signals in subjects remitted fro... | ||
Medical condition: Cognitive dysfunction Major depressive disorder (MDD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000219-15 | Sponsor Protocol Number: 13-10 | Start Date*: 2014-11-27 |
Sponsor Name:VU Medical Center | ||
Full Title: Amyloid pathology in cognitively normal elderly subjects | ||
Medical condition: Cognitively healthy elderly, aged 60-100 years old. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002171-11 | Sponsor Protocol Number: 010622 | Start Date*: 2024-07-02 |
Sponsor Name:Medical University of Łódź | ||
Full Title: Randomized, double-blind, placebo-controlled trial evaluating efficacy and safety of dimethyl fumarate in brain atrophy reduction, synaptic functional connectivity, cognitive functions, quality of ... | ||
Medical condition: dementia and mild cognitice impairment due to Alzheimer's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000492-17 | Sponsor Protocol Number: NL39440.029.10 | Start Date*: 2012-10-29 |
Sponsor Name:Afdeling Klinische Neuropsychologie Vrije Universiteit Amsterdam | ||
Full Title: The Effects of Long-acting Methylphenidate on Academic Activity and Related Constructs in Children with ADHD: A Randomised Placebo Controlled Trial | ||
Medical condition: Attention-deficit hyperactivity disorder (ADHD) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000258-64 | Sponsor Protocol Number: D1449L00004 | Start Date*: 2005-04-08 |
Sponsor Name:AstraZeneca AB | ||
Full Title: SCORE An open, randomised, parallel, three treatment groups, multicentre, phase IV study - in real life - to compare the change in social outcome of quetiapine fumarate (Seroquel®) combined with Co... | ||
Medical condition: Schizophrenia is a chronic psychiatric disorder that often begins during adolescence or early adulthood. A major problem for patients with schizophrenia is a cognitive deficit compared to a control... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002213-19 | Sponsor Protocol Number: ELICE-BD-O1 | Start Date*: 2019-09-19 | |||||||||||
Sponsor Name:University of British Columbia | |||||||||||||
Full Title: A 6-Week Randomised, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy of Lurasidone Adjunctive Therapy in Improving Cognitive Functioning in Euthymic Bipolar Disorder Pa... | |||||||||||||
Medical condition: Euthymic Bipolar disorder | |||||||||||||
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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) |
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