- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25 result(s) found for: False neurotransmitter.
Displaying page 1 of 2.
EudraCT Number: 2019-003032-23 | Sponsor Protocol Number: AADC-010 | Start Date*: 2019-10-09 |
Sponsor Name:National Taiwan University Hospital | ||
Full Title: A Phase I/II Clinical Trial for Treatment of Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency Using AAV2-hAADC | ||
Medical condition: Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2019-003072-39 | Sponsor Protocol Number: NTUH-AADC-011 | Start Date*: 2019-10-09 |
Sponsor Name:National Taiwan University Hospital | ||
Full Title: A Clinical Trial for Treatment of Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency Using AAV2-hAADC - An Expansion | ||
Medical condition: Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-002977-12 | Sponsor Protocol Number: EPUP81 | Start Date*: 2014-10-08 |
Sponsor Name:Maastriccht University | ||
Full Title: BRAIN KINETICS OF NEUROTRANSMISSION DURING THC INTOXICATION | ||
Medical condition: Brain functioning during THC intoxication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000353-21 | Sponsor Protocol Number: substance P | Start Date*: 2006-05-29 |
Sponsor Name:Cliniques Universitaire St Luc | ||
Full Title: Comparison of the vasoreactivity and endogenous NO production between the left and right internal mammary 6 months after bypass surgery with the injection of substance P and exogenous nitric oxide. | ||
Medical condition: We observe a higher FFR in the RITA then in the LIMA 6 month after CABG (Glineur D, Resistance to flow of arterial Y-grafts 6 months after coronary artery bypass surgery.Circulation. 2005 Aug 30;1... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000063-25 | Sponsor Protocol Number: AX-CL-09e | Start Date*: 2005-06-10 | |||||||||||
Sponsor Name:Axonyx Inc | |||||||||||||
Full Title: A 26 week double-blind extension to a 26 week randomised, double-blind placebo-controlled study that evaluated the safety and efficacy of two different doses of phenserine-tartrate in patients with... | |||||||||||||
Medical condition: Alzheimer's disease is caused by a loss of nerve cells in the brain, particularly in the areas associated with memory and learning. The onset of Alzheimer's also affects the levels of a certain ne... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002211-24 | Sponsor Protocol Number: VITC-001 | Start Date*: 2006-10-27 |
Sponsor Name:FAZ - Floridsdorf Allergy Center | ||
Full Title: Wirksamkeit von oralem Vitamin C bei der Seekrankheit | ||
Medical condition: Die Seekrankheit (motion sickness) stellt ein weiterhin aktuelles Problem in der professionellen wie nicht-professionellen Seefahrt sowie auch beim Transport mit anderen Fortbewegungsmitteln (Auto,... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002836-30 | Sponsor Protocol Number: 22218MFPF-Weave | Start Date*: 2023-03-15 |
Sponsor Name:Vrije Universiteit Brussel | ||
Full Title: Investigating fundamental mechanisms of mental and physical fatigue using neurotransmitter reuptake inhibitors and electroencephalography: a randomized counterbalanced crossover trial | ||
Medical condition: Acute mental and physical fatigue in healthy participants | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004004-20 | Sponsor Protocol Number: UI04/6748 | Start Date*: 2005-09-26 |
Sponsor Name:University of Leeds | ||
Full Title: A Randomised, Double-blind, Placebo Controlled trial to test the efficacy of St John's Wort (Hypericum Perforatum) for Premenstrual Syndrome. | ||
Medical condition: The 'premenstrual syndrome' is a cyclical condition occurring 7-10 days before the onset of menstruation, and is relieved at, or shortly after commencement of menstrual flow. The most commonly repo... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-000089-11 | Sponsor Protocol Number: AX-CL-09 | Start Date*: 2004-12-15 |
Sponsor Name:Axonyx Inc | ||
Full Title: A randomised, double-blind, placebo-controlled study to evaluate the safety and efficacy of two different doses of phenserine-tartrate in patients with probable mild to moderate Alzheimer’s disease | ||
Medical condition: Alzheimer's Disease is caused by a loss of nerve cells in the brain, particularly in the areas associated with memory and learning. The onset of Alzheimer's also affects the levels of a certain neu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000933-12 | Sponsor Protocol Number: AX-CL-10 | Start Date*: 2005-02-22 |
Sponsor Name:Axonyx Inc | ||
Full Title: A randomised, double-blind, placebo-controlled study to evaluate the safety and efficacy of two different doses of phenserine-tartrate in patients with probable mild to moderate Alzheimer’s disease | ||
Medical condition: Alzheimers disease is caused by a loss of nerve cells in the brain, particularly in the areas associated with memory and learning. The onset of Alzheimers's also affects the levels of a certain neu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000794-31 | Sponsor Protocol Number: October2011,version5 | Start Date*: 2011-06-15 | |||||||||||
Sponsor Name:Dept. of Pharmacology | |||||||||||||
Full Title: Neurodegenerative Changes in Alzheimer’s Disease: Identifying potential effects of Victoza® on degenerative changes | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011824-79 | Sponsor Protocol Number: 91686125 | Start Date*: 2009-11-03 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Effects of fluoxetine on the outgrowth of the serotonergic system | |||||||||||||
Medical condition: We investigate whether the effects fluoxetine (Prozac®) on the outgrowth of the serotonergic system are dependent on age. In a 16 week multicenter randomized, double-blind, placebo controlled trial... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003975-38 | Sponsor Protocol Number: TERPAH-001 | Start Date*: 2007-11-22 | |||||||||||
Sponsor Name:Ergonex Pharma GmbH | |||||||||||||
Full Title: Proof of Concept Study to Investigate the Efficacy, Haemodynamics and Tolerability of Terguride vs. Placebo in Patients with Pulmonary Arterial Hypertension. Double-blind, randomized, prospective P... | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000097-35 | Sponsor Protocol Number: CCFZ533X2204 | Start Date*: 2015-09-02 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo-controlled, parallel group study to preliminarily evaluate the safety, tolerability, pharmacokinetics and efficacy of CFZ533 in patients with moder... | |||||||||||||
Medical condition: Acquired myasthenia gravis (MG) is an autoimmune disease that leads to fluctuating muscle weakness and fatigue. In the most common cases, muscle weakness is caused by circulating antibodies that bi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001076-58 | Sponsor Protocol Number: 191622-145 | Start Date*: 2015-01-14 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: BOTOX® Efficacy and Safety in the Treatment of Knee Osteoarthritis | |||||||||||||
Medical condition: Knee Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002002-20 | Sponsor Protocol Number: 2014METAL1 | Start Date*: 2015-06-10 |
Sponsor Name:UMCG | ||
Full Title: A multicentre randomized double-blind placebo controlled discontinuation trial of methylphenidate | ||
Medical condition: attention-deficit/hyperactivity disorder | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004006-18 | Sponsor Protocol Number: ParkinsonDPI-3 | Start Date*: 2018-06-07 | |||||||||||
Sponsor Name:Pharmaceutical Technology and Biopharmacy, University of Groningen | |||||||||||||
Full Title: Therapeutic effects of an inhaled levodopa dry powder formulation on the recovery from off periods in patients with Parkinson's disease | |||||||||||||
Medical condition: Parkinson's disease is a progressive neurodegenerative disorder characterized by a lack of dopamine production due to the loss of dopamine producing cells in the substantia nigra. This lack of dopa... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002768-25 | Sponsor Protocol Number: 191622-102 | Start Date*: 2011-11-10 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: A Single Center, Double-blind, Randomized, Placebo-controlled, Parallel-group Study of the Efficacy and Safety of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex as Treatment for Osteoa... | |||||||||||||
Medical condition: Treatment of Osteoarthritis Knee Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003080-38 | Sponsor Protocol Number: GOAT_1-2_1407 | Start Date*: 2015-06-26 |
Sponsor Name: Radboud University Nijmegen Medical Centre, Donders Institute for Brain, Cognition and Behaviour | ||
Full Title: Glutamatergic medication in the treatment of Obsessive Compulsive Disorder (OCD) and Autism Spectrum Disorder (ASD) | ||
Medical condition: - Obsessive-compulsive disorder - Autistic Diorder, Aspergers' Disorder, PDD NOS | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2007-000579-40 | Sponsor Protocol Number: D1443L00002 | Start Date*: 2007-10-10 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: Effects of atypical versus typical neuroleptics on motivation, hedonia, and social cognition in patients with schizophrenia – an fMRI study | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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