- Trials with a EudraCT protocol (1,111)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
1,111 result(s) found for: Brain function.
Displaying page 5 of 56.
EudraCT Number: 2020-000160-28 | Sponsor Protocol Number: MusicPlasticity | Start Date*: 2020-08-28 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Investigation of SSRI induced neuroplastic changes in musicians using functional magnetic resonance imaging | ||
Medical condition: Focal dystonia in musicians | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001836-69 | Sponsor Protocol Number: Vort-MCI_001 | Start Date*: 2021-09-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effects of Vortioxetine in Mild Cognitive Impairment measured by Functional Magnetic Resonance Imaging | ||
Medical condition: Mild cognitive impairment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002318-11 | Sponsor Protocol Number: 109MS306 | Start Date*: 2014-06-05 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: Open-Label, Randomized, Multicenter, Multiple-Dose, Active Controlled, Parallel-Group, Efficacy and Safety Study of BG00012 in Children From 10 to Less Than 18 Years of Age With Relapsing-Remitting... | ||||||||||||||||||
Medical condition: Relapsing-Remitting Multiple Sclerosis | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) BE (Completed) IT (Completed) HU (Completed) DK (Completed) CZ (Completed) PL (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) FR (Trial now transitioned) DE (Completed) BG (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004373-50 | Sponsor Protocol Number: 369852 | Start Date*: 2021-04-08 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Effect of treatment with Semaglutide on cognitive function, neuroinflammation and hepatic nitrogen metabolism in patients with non-alcoholic steatohepatitis: A randomized placebo-controlled trial | |||||||||||||
Medical condition: Non-alcoholic steatohepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004010-28 | Sponsor Protocol Number: I3Y-MC-JPBO | Start Date*: 2015-03-10 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2 Study of Abemaciclib in Patients with Brain Metastases Secondary to Hormone Receptor Positive Breast Cancer, Non-small Cell Lung Cancer, or Melanoma | |||||||||||||
Medical condition: Brain tumors, Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005212-40 | Sponsor Protocol Number: MR080508 | Start Date*: 2008-10-14 | ||||||||||||||||||||||||||
Sponsor Name:Karolinska Institute | ||||||||||||||||||||||||||||
Full Title: Pain mechanisms and fatigue in rheumatoid arthritis (RA) and healthy volunteers. Can antirheumatic and biological therapy affect pain processing and fatigue in RA? | ||||||||||||||||||||||||||||
Medical condition: Rheumatoid arthritis (RA) The overall aim with this project is to investigate central pain mechanisms in RA and healthy controls, and in RA how these are influenced by autonomic neural regulation ... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001953-33 | Sponsor Protocol Number: PrevSVD-2015 | Start Date*: 2015-10-09 | |||||||||||||||||||||||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||||||||||||||||||||||
Full Title: Preventing cognitive decline and dementia from cerebral small vessel disease | |||||||||||||||||||||||||||||||||
Medical condition: Lacunar (small vessel) ischaemic stroke | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002491-39 | Sponsor Protocol Number: SGNTUC-028 | Start Date*: 2022-02-11 | |||||||||||||||||||||
Sponsor Name:Seagen Inc. | |||||||||||||||||||||||
Full Title: A randomized, double-blind, phase 3 study of tucatinib or placebo in combination with trastuzumab and pertuzumab as maintenance therapy for metastatic HER2+ breast cancer (HER2CLIMB-05) | |||||||||||||||||||||||
Medical condition: Unresectable locally-advanced or metastatic HER2+ breast cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) PT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) IT (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) GR (Trial now transitioned) CZ (Trial now transitioned) FI (Trial now transitioned) NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004435-30 | Sponsor Protocol Number: SC06-02 | Start Date*: 2006-10-31 | |||||||||||
Sponsor Name:FONDAZIONE SANTA LUCIA | |||||||||||||
Full Title: Protocol of study for the evaluation of the efficacy of rivastigmine on cognitive and behavioural disorders, following traumatic brain injury TBI in chronic patients. | |||||||||||||
Medical condition: Patients with cognitive and behavioural disorders following severe TBI and other severe acquired brain injury Glasgow Coma Scale GCS lower or equal 8 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004007-12 | Sponsor Protocol Number: 066VER | Start Date*: 2020-06-02 |
Sponsor Name:University of Sussex | ||
Full Title: Brain connectivity and patient reported outcomes in people with HIV (PWH) with symptoms of insomnia switching integrase inhibitor-based ART; a randomised controlled study | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001532-11 | Sponsor Protocol Number: 01apr2014 | Start Date*: 2014-09-11 |
Sponsor Name:Ospedale San Raffaele | ||
Full Title: MONO-INSTITUTIONAL PHASE II TRIAL ADDRESSING TOLERABILITY AND ACTIVITY OF R-CHOP CHEMOIMMUNOTHERAPY PRECEDED BY BLOOD-BRAIN BARRIER PERMEABILIZATION BY NGR-TUMOR NECROSIS FACTOR IN PATIENTS WITH RE... | ||
Medical condition: Primary non-Hodgkin lymphoma in the central nervous system relapse / refractory | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001684-21 | Sponsor Protocol Number: NV1205-009 | Start Date*: 2018-04-20 |
Sponsor Name:Neurov Acquisition LLC | ||
Full Title: Phase I/II, Open-Label, Dose Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of NV1205 in Pediatric Male Subjects with Childhood Cerebral Adrenoleukodystrophy (CCALD) | ||
Medical condition: Childhood Cerebral Adrenoleukodystrophy (CCALD) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male | |
Trial protocol: GB (Prematurely Ended) FR (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2012-005723-33 | Sponsor Protocol Number: amantadineSCEDI. | Start Date*: 2015-03-27 |
Sponsor Name:GGZ Oost Brabant | ||
Full Title: Efficacy of amantadine on behavioural and emotional problems and impairment of executive functioning due to acquired brain injury to the frontal lobes: a series of single case experimental design s... | ||
Medical condition: behavioural and emotional problems and impairment of executive functioning due to acquired brain injury to the frontal lobes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005345-11 | Sponsor Protocol Number: RA2364 | Start Date*: 2007-08-08 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: ‘Stem cell Trial of recovery EnhanceMent after Stroke 2’ (STEMS2) pilot randomised placebo-controlled trial of granulocyte-colony stimulating factor in mobilising bone marrow stem cells in sub-acu... | |||||||||||||
Medical condition: Ischaemic and Haemorrhagic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022737-28 | Sponsor Protocol Number: CO10/9344 | Start Date*: 2011-02-03 |
Sponsor Name:Leeds Teaching Hospitals NHS Trust | ||
Full Title: A randomised phase II screening trial with functional imaging and patient reported toxicity sub-studies comparing LApatiNib plus capecitabine versus continued Trastuzumab plus capecitabine after lo... | ||
Medical condition: Patients with ERB B2 positive metastatic breast cancer developing brain metastasis/es | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-006195-39 | Sponsor Protocol Number: EarlyAD-PET | Start Date*: 2012-02-29 | |||||||||||||||||||||
Sponsor Name:Skånes universitetssjukhus | |||||||||||||||||||||||
Full Title: An open-label study to compare the prognostic value of (18F)Flutemetamol PET-imaging with longitudinal biomarker data in healthy volunteers and patients with mild cognitive impairment | |||||||||||||||||||||||
Medical condition: Dementia and cognitive impairment; in particular mild cognitive impairment and Alzheimer's disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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: 2019-000617-37 | Sponsor Protocol Number: NL68690.091.18 | Start Date*: 2019-07-11 |
Sponsor Name:Rijnstate ziekenhuis | ||
Full Title: StudY of effect of Nimodipine and Acetaminophen on Postictal Symptoms after ECT | ||
Medical condition: Postictal phenomena after electroconvulsive therapy (ECT) induced seizures. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002656-14 | Sponsor Protocol Number: 1733 | Start Date*: 2012-06-11 |
Sponsor Name:Imperial College | ||
Full Title: A randomised, prospective study, assessing changes in cerebral function in treatment naive HIV-1 infected subjects commencing either boosted atazanavir with Truvada or boosted darunavir with maravi... | ||
Medical condition: HIV infection and cognitive function | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005041-33 | Sponsor Protocol Number: MAG111539 | Start Date*: 2009-07-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Single-Blind Study of the Safety, Pharmacokinetics and Pharmacodynamics of Escalating Repeat Doses of GSK249320 in Patients With Stroke. | |||||||||||||
Medical condition: Patients with Stroke. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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