- Trials with a EudraCT protocol (46)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
46 result(s) found for: Task analysis.
Displaying page 1 of 3.
| EudraCT Number: 2018-003945-40 | Sponsor Protocol Number: EPU-P112 | Start Date*: 2019-04-10 |
| Sponsor Name:Maastricht University | ||
| Full Title: EFFECTS OF VAPORISED CANNABIS, WITH AND WITHOUT CBD, ON DRIVING AND COGNITION | ||
| Medical condition: This study will look at the differential effects of variations in cannabis chemovars on driving ability and cognition | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-024543-33 | Sponsor Protocol Number: P64 | Start Date*: 2011-04-14 |
| Sponsor Name:Maastricht University | ||
| Full Title: Can memantine prevent memory impairment induced by MDMA in humans | ||
| Medical condition: none | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003049-13 | Sponsor Protocol Number: 7347 | Start Date*: 2022-08-24 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: EEG-MRI study of the effect of methylphenidate on neural mechanisms in adult patients with ADHD with or without mood disorders: A randomized controlled trial versus placebo. | ||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| 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: 2014-004650-34 | Sponsor Protocol Number: GR-2011-02348985 | Start Date*: 2016-06-27 | |||||||||||
| Sponsor Name:IRCCS FONDAZIONE ISTITUTO NEUROLOGICO NAZIONALE C. MONDINO | |||||||||||||
| Full Title: Neuromodulation strategies to enhance the effects of gait rehabilitation in multiple sclerosis patients with cerebellar ataxia | |||||||||||||
| Medical condition: Multiple sclerosis with cerebellar ataxia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012141-34 | Sponsor Protocol Number: ORTH-016 | Start Date*: 2009-06-29 |
| Sponsor Name:University Hospital of North Tees and Hartlepool | ||
| Full Title: Randomised Controlled Trial of the Use of Topical Application of Tranexamic Acid in Primary Total Hip Replacement. | ||
| Medical condition: Blood loss in total hip replacement in patient with ostoearthritis and rheumatoid arthritis. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| 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: 2021-000058-24 | Sponsor Protocol Number: Connect&Go | Start Date*: Information not available in EudraCT |
| Sponsor Name:Erasmus MC Cancer Institute | ||
| Full Title: Administration of immune checkpoint inhibitors through an elastomeric pump. A patient preference study and cost analysis. | ||
| Medical condition: Solid tumors for which nivolumab or pembrolizumab monotherapy is an EMA approved indication. This includes (but is not limited to) melanoma, renal-cell cancer, NSCLC and head and neck cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-022857-41 | Sponsor Protocol Number: C6930943 | Start Date*: 2010-12-14 | |||||||||||
| Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
| Full Title: Effects of a common cold treatment on cognitive function | |||||||||||||
| Medical condition: Common cold | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000307-17 | Sponsor Protocol Number: DIAN-TU-001 | Start Date*: 2014-01-08 |
| Sponsor Name:Washington University in St. Louis | ||
| Full Title: A Phase II/III randomized, double-blind, placebo-controlled, cognitive endpoint, multicenter study of potential disease modifying therapies in individuals at risk for and with dominantly inherited ... | ||
| Medical condition: Dominantly Inherited Alzheimer Disease (DIAD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Trial now transitioned) ES (Temporarily Halted) DE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001461-36 | Sponsor Protocol Number: CT-AMT-130-02 | Start Date*: 2021-06-30 | |||||||||||
| Sponsor Name:uniQure biopharma B.V. | |||||||||||||
| Full Title: A Phase Ib/II Randomised, Double-Blind Study to Explore Safety, Tolerability, and Efficacy Signals of Multiple Doses of Striatally-Administered rAAV5-miHTT Total Huntingtin Gene (HTT) Lowering Ther... | |||||||||||||
| Medical condition: Huntington Disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2020-000829-55 | Sponsor Protocol Number: PSILO4ALCO | Start Date*: 2020-12-16 | ||||||||||||||||
| Sponsor Name:Psychiatric Centre Copenhagen | ||||||||||||||||||
| Full Title: Can a one-off administration of psilocybin reduce alcohol intake in patients with alcohol use disorder? A randomized, double-blinded, placebo-controlled clinical trial. | ||||||||||||||||||
| Medical condition: Alcohol Use Disorder | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-013420-23 | Sponsor Protocol Number: F1J-US-HMGO | Start Date*: 2009-11-09 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Neurobiological Correlates of Antidepressant Response After Duloxetine Hydrochloride Treatment in Subjects with Major Depressive Disorder | |||||||||||||
| Medical condition: Major depressive disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004129-89 | Sponsor Protocol Number: Motor-Neuromod_01, Part I-III | Start Date*: 2005-09-19 |
| Sponsor Name:Universitätsklinikum Münster | ||
| Full Title: Potentiation of procedural motor learning by pharmacological neuromodulation and brain stimulation | ||
| Medical condition: Healthy volunteers Patients in the chronic stage (> 1 year) after stroke | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004487-25 | Sponsor Protocol Number: KETASELF-1 | Start Date*: 2021-02-08 |
| Sponsor Name:Linköpings Universitet | ||
| Full Title: Experiencing the self through touch - self-other-distinction in an altered state of self: An exploratory randomized placebo-controlled experimental medicine study | ||
| Medical condition: Healthy volunteer. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003219-22 | Sponsor Protocol Number: LMS/SF/UH/0018 | Start Date*: 2014-01-27 | |||||||||||
| Sponsor Name:Hertfordshire Partnership University NHS Foundation Trust [...] | |||||||||||||
| Full Title: A randomised controlled feasibility trial comparing clinical and cost effectiveness of cognitive behavioural therapy (CBT) and selective serotonin reuptake inhibitors (SSRI) and their combination i... | |||||||||||||
| Medical condition: Obsessive Compulsive Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001818-14 | Sponsor Protocol Number: RELATE-TRD | Start Date*: 2013-12-20 | |||||||||||
| Sponsor Name:University Medical Center Groningen | |||||||||||||
| Full Title: RELATE and PREDICT TRD A pharmacological and neuroimaging study investigating neurobiological effects of Selective Serotonin Reuptake Inhibitors and Norepinephrine Reuptake inhibitors on dopaminer... | |||||||||||||
| Medical condition: Major Depressive Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004241-36 | Sponsor Protocol Number: ML42502 | Start Date*: 2021-03-23 | |||||||||||
| Sponsor Name:Roche Farma S.A | |||||||||||||
| Full Title: TIME AND MOTION STUDY OF A SUBCUTANEOUS FIXED-DOSE COMBINATION OF PERTUZUMAB AND TRASTUZUMAB FOR THE TREATMENT OF PATIENTS WITH HER2-POSITIVE EARLY BREAST CANCER. | |||||||||||||
| Medical condition: EARLY BREAST CANCER | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005995-37 | Sponsor Protocol Number: COAV101A12306 | Start Date*: 2021-08-25 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A Phase lllb, open-label, single-arm, single-dose, multicenter study to evaluate the safety, tolerability and efficacy of gene replacement therapy with intravenous OAV101 (AVXS-101) in pediatric pa... | |||||||||||||
| Medical condition: Spinal Muscular Atrophy | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) BE (Completed) PT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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