- Trials with a EudraCT protocol (68)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
68 result(s) found for: Structural brain disorders.
Displaying page 1 of 4.
| EudraCT Number: 2008-003059-56 | Sponsor Protocol Number: ICAND | Start Date*: 2008-07-29 | |||||||||||
| Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
| Full Title: Phase II trial to assess safety and efficacy of Iron chelating agent Deferiprone in patients with Pantothenate Kinase-Associated Neurodegeneration ICAND Trial | |||||||||||||
| Medical condition: PKAN | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004509-30 | Sponsor Protocol Number: 012020 | Start Date*: 2021-05-13 | |||||||||||
| Sponsor Name:INSTITUTO DE ESTUDIOS DE CIENCIAS DE LA SALUD DE CASTILLA Y LEON | |||||||||||||
| Full Title: A prospective structural, diffusion and connectomics MRI study on migraine patients treated with Fremanezumab | |||||||||||||
| Medical condition: MIGRAINE | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004172-17 | Sponsor Protocol Number: ETES | Start Date*: 2021-04-26 |
| Sponsor Name:Medizinische Universität Innsbruck | ||
| Full Title: Electroconvulsive therapy vs. esketamine nasal spray in treatment-resistant depression: a longitudinal, randomized efficacy comparison pilot study | ||
| Medical condition: treatment resistant depression | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-006176-16 | Sponsor Protocol Number: I5Q-NS-O001 | Start Date*: 2022-09-26 | |||||||||||
| Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
| Full Title: Definition of neuroimaging and laboratory biomarkers as possible predictors for treatment response to Galcanezumab in high-frequency episodic migraine (PREDICT) | |||||||||||||
| Medical condition: High-frequency episodic migraine. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001217-25 | Sponsor Protocol Number: 2016-001217-25 | Start Date*: 2016-09-07 |
| Sponsor Name:Uppsala University | ||
| Full Title: Emotion, Serotonin and Premenstrual Dysphoric Disorder (EmSeP) | ||
| Medical condition: Premenstrual Dysphoric Disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004984-31 | Sponsor Protocol Number: DR180133 | Start Date*: 2021-04-21 |
| Sponsor Name:CHRU TOURS | ||
| Full Title: Nitrous Oxide in Resistant Depression in Elderly Subjects: A Randomized, Double-blind, Comparator Trial | ||
| Medical condition: Resistant Depression in the Elderly Subject | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003128-19 | Sponsor Protocol Number: BiCS2019 | Start Date*: 2019-11-27 | |||||||||||
| Sponsor Name:Psykiatrisk Center Glostrup | |||||||||||||
| Full Title: Biomarkers in Clozapine-responding Schizophrenia | |||||||||||||
| Medical condition: schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| 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: 2021-000442-18 | Sponsor Protocol Number: ABM/2020/1/00002 | Start Date*: 2021-09-24 | ||||||||||||||||
| Sponsor Name:National Institute of Cardiology | ||||||||||||||||||
| Full Title: Strategy To Optimize PeriproCeduraL AnticOagulation in Structural Transseptal Interventions (STOP CLOT Trial) | ||||||||||||||||||
| Medical condition: Mitral regurgitation Atrial fibrilation Periprocedural anticoagulation strategy in patients treated with MitraClip implantation or Left Atrial Appendage Closure. The patients scheduled for Mitr... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2007-004025-20 | Sponsor Protocol Number: TMT110684 | Start Date*: 2007-10-04 | |||||||||||
| Sponsor Name:GlaxoSmithKline | |||||||||||||
| Full Title: A randomised, double-blind, parallel-group, fixed-dose, placebo-controlled study comparing correlates of brain functional activation before and after treatment with placebo and Paroxetine in partic... | |||||||||||||
| Medical condition: Major Depressive Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002636-13 | Sponsor Protocol Number: 001 | Start Date*: 2017-04-28 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Study of Antithrombotic Treatment after Intracerebral Haemorrhage (STATICH) | ||
| Medical condition: We want to study patients with indication for antithrombotic drugs who suffers from spontaneous intracerebral hemorrhage (ICH). It has long been unclear whether survivors of ICH should start antith... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) NO (Prematurely Ended) DK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003286-34 | Sponsor Protocol Number: CHUBX2017/22 | Start Date*: 2019-03-05 | ||||||||||||||||
| Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
| Full Title: In vivo involvement of the cholinergic and dopaminergic systems in the pathophysiology of apathy. | ||||||||||||||||||
| Medical condition: Apathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-006042-32 | Sponsor Protocol Number: GE-067-019 | Start Date*: 2012-09-12 | |||||||||||
| Sponsor Name:GE Healthcare Ltd and its affiliates | |||||||||||||
| Full Title: A Single-Arm Open-Label Multi-Center Study to Determine the Test-Retest Variability of PET Brain Imaging with Flutemetamol (18F) Injection. | |||||||||||||
| Medical condition: Subjects with amnestic Mild Cognitive Impairment (aMCI) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000712-30 | Sponsor Protocol Number: ABR-71432 | Start Date*: 2021-06-07 | |||||||||||
| Sponsor Name:Radboudumc | |||||||||||||
| Full Title: Targeted glucocorticoid administration to improve safety learning in PTSD patients with HPA axis dysregulation | |||||||||||||
| Medical condition: Posttraumatic Stress Disorder (PTSD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005124-18 | Sponsor Protocol Number: LUMC-NEUR-0001 | Start Date*: 2012-07-12 | |||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||
| Full Title: Chronification and reversibility of migraine | |||||||||||||
| Medical condition: Patients suffering from chronic migraine and medication overuse | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003191-39 | Sponsor Protocol Number: | Start Date*: 2013-01-21 | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: The effect of a single-dose of d-cycloserine on the basic effects of cognitive-behaviour therapy for panic disorder - a randomized placebo-controlled trial | |||||||||||||
| Medical condition: DSM-IV Panic disorder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002631-42 | Sponsor Protocol Number: MS700568_0022 | Start Date*: 2018-04-18 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: A 2-year prospective study to evaluate the onset of action of Mavenclad® in subjects with highly active relapsing multiple sclerosis | |||||||||||||
| Medical condition: Relapsing multiple sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) HU (Completed) AT (Completed) CZ (Completed) ES (Completed) FR (Completed) BE (Completed) FI (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000123-33 | Sponsor Protocol Number: RH EPOA-REHAB | Start Date*: 2011-06-01 | |||||||||||
| Sponsor Name:King's College Hospital NHS Foundation Trust [...] | |||||||||||||
| Full Title: Evaluation of the feasibility of modulating and measuring endogenous neurogenesis with erythropoietin (rhEPOα) to expedite recovery after stroke | |||||||||||||
| Medical condition: Stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001288-58 | Sponsor Protocol Number: 40122 | Start Date*: 2012-05-21 | |||||||||||
| Sponsor Name:Academic Medical Center | |||||||||||||
| Full Title: Boosting oxytocin after trauma: The effects of intranasal oxytocin administration on emotional and motivational brain processes in PTSD | |||||||||||||
| Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001554-18 | Sponsor Protocol Number: 13-082 | Start Date*: 2016-08-31 |
| Sponsor Name:RWTH Aachen University represented by the Rector, represented by the Dean of the Medical Faculty | ||
| Full Title: English: Are Antipsychotics Neurotoxic or Neuroprotective? A Randomised Multicentre Longitudinal Study for Comparison of Two Therapy Strategies for the Treatment of Schizophrenia. | ||
| Medical condition: Schizophrenia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
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