- Trials with a EudraCT protocol (217)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
217 result(s) found for: Pharmacological effect.
Displaying page 1 of 11.
EudraCT Number: 2018-002637-37 | Sponsor Protocol Number: NL66693.058.18 | Start Date*: 2020-06-29 |
Sponsor Name:Leiden University | ||
Full Title: Manipulating NMDA-dependent learning to alter nocebo effects: A pharmacological fMRI study on pain and itch. | ||
Medical condition: Nocebo effects on pain and itch | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004812-73 | Sponsor Protocol Number: BP18-1-501 | Start Date*: 2022-05-16 |
Sponsor Name:Leiden University | ||
Full Title: The influence of pharmacological conditioning with S-ketamine on pain sensitivity in patients with Fibromyalgia Syndrome | ||
Medical condition: Fibromyalgia Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001384-11 | Sponsor Protocol Number: captaf | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Catheter Ablation compared with Pharmacological Therapy for Atrial Fibrillation – the CAPTAF trial | |||||||||||||
Medical condition: To study the effect of catheter ablation (using CE marked products) on the quality of life an in patients with atrial fibrillation depsite treatment with conevntional antiarrhythmic medical therapy... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005087-93 | Sponsor Protocol Number: | Start Date*: 2006-11-17 |
Sponsor Name:East Kent Hospitals NHS Trust | ||
Full Title: A randomized double blind placebo controlled trial of Memantine in the treatment of Agitation in Alzheimers Dementia | ||
Medical condition: Alzheimers dementia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002890-37 | Sponsor Protocol Number: 1 | Start Date*: 2017-02-07 | |||||||||||
Sponsor Name:Esther Aleo Lujan | |||||||||||||
Full Title: Double-blind randomized clinical trial to compare presurgery anxiolysis in children treated with hydroxyzine versus non-pharmacological intervention (distractoria technique clown). | |||||||||||||
Medical condition: Presurgery anxiety | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002289-62 | Sponsor Protocol Number: ST200-SSMA-14-001 | Start Date*: 2014-09-11 | |||||||||||
Sponsor Name:SIGMA-TAU, Industrie Farmaceutiche Riunite S.p.A. | |||||||||||||
Full Title: Electroneurographic and clinical evaluation in patients with mild / moderate Carpal Tunnel Syndrome , following conservative pharmacological treatment with Nicetile®. | |||||||||||||
Medical condition: Carpal Tunnel Syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000287-17 | Sponsor Protocol Number: RC12-01 | Start Date*: 2012-05-21 | |||||||||||
Sponsor Name:FONDAZIONE SANTA LUCIA | |||||||||||||
Full Title: PROMOTION OF FUNCTIONAL RESTORATION THROUGH PHARMACOLOGICAL MODULATION OF BRAIN PLASTICITY WITH AMINOPYRIDINE IN PATIENTS WITH MULTIPLE SCLEROSIS STUDIED BY FUNCTIONAL MRI | |||||||||||||
Medical condition: Patients with MS, without relevant medical conditions, with right upper limb impairment assessed by a hand dexterity test will be included.Patients will be in a non-active phase of the disease and ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001291-71 | Sponsor Protocol Number: W005PS0208_1 | Start Date*: 2008-07-23 |
Sponsor Name:University of Wuerzburg | ||
Full Title: Electrophysiological correlates of putative endophenotypes of attention-deficit / hyperactivity disorder (ADHD) | ||
Medical condition: Attention-deficit hyperactivity disorder (ADHD) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001066-14 | Sponsor Protocol Number: DENERVHTA | Start Date*: 2012-07-17 |
Sponsor Name:Consorci Mar Parc de salut de Barcelona ( Parc de Salut Mar) | ||
Full Title: Sympathetic renal denervation versus increment of pharmacological treatment in resistant arterial hypertension | ||
Medical condition: subjects with resistant hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004548-31 | Sponsor Protocol Number: HUB-PSI-CAMAD | Start Date*: 2020-04-18 | ||||||||||||||||
Sponsor Name:Cinto Segalàs | ||||||||||||||||||
Full Title: A RANDOMIZED, CONTROLLED, OPEN AND UNICENTRIC PHASE II CLINICAL TRIAL, WITH TWO PARALLEL GROUPS, TO EVALUATE THE ANTIDEPRESSANT EFFICACY OF PSYCHOTHERAPY AND CITALOPRAM IN WOMEN DIAGNOSED WITH BREA... | ||||||||||||||||||
Medical condition: Female patients diagnosed with breast cancer who, during the first year following the diagnosis of oncological disease, have affective symptomatology that meets DSM-V criteria for major depression. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-004350-91 | Sponsor Protocol Number: TAK-375/EC301 | Start Date*: 2005-11-10 | |||||||||||
Sponsor Name:Takeda Europe R&D Centre Ltd | |||||||||||||
Full Title: A multicentre, randomised, double-blind, double-dummy, placebo-controlled study to evaluate the safety and efficacy of ramelteon compared to placebo with zopiclone as a reference arm in adults with... | |||||||||||||
Medical condition: chronic insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) FI (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002755-42 | Sponsor Protocol Number: 1069/12 | Start Date*: 2012-11-06 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: OBESITY AND ASPIRIN RESPONSIVENESS | |||||||||||||
Medical condition: OBESITY | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000483-29 | Sponsor Protocol Number: Wada_2012 | Start Date*: 2013-07-17 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: The influence of exercise and hydration to the pharmacological response to inhaled terbutalin and salbutamol in men | |||||||||||||
Medical condition: To investigate the pharmacokinetic effect of the medicine under physical work in healthy men | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000230-39 | Sponsor Protocol Number: FOG 2006 | Start Date*: 2008-04-14 |
Sponsor Name:Endocrine Society of Czech Republic | ||
Full Title: Protective effect of gonadoliberin analogues on endocrine and reproduction ovarian function during antitumour treatment in young girls and women in fertile period: Project of pharmacological gonada... | ||
Medical condition: The patient with diagnosis: Hodgkin disease and leukaemia. Patients starting at adolescence (B3 - B4 for breast development accordig Tanner criteria) till 34 years be included. ... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001659-42 | Sponsor Protocol Number: ANTITROMBINA | Start Date*: 2020-04-18 | ||||||||||||||||
Sponsor Name:Fundación para la Investigación Biomédica de Córdoba | ||||||||||||||||||
Full Title: Pilot study of antithrombin as prophylaxis of acute respiratory distress syndrome in patients with COVID-19 | ||||||||||||||||||
Medical condition: Confirmed SARS-CoV-2 respiratory infection with poor prognostic factors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000650-21 | Sponsor Protocol Number: PHARMADIPOAGE | Start Date*: 2018-10-31 | |||||||||||
Sponsor Name:Universidad Autónoma de Madrid | |||||||||||||
Full Title: CLINICAL TRIAL FOR EVALUATION OF THE ADIPOQUINAS: NEW PHARMACOLOGICAL TARGETS TO PREVENT VASCULAR AGING | |||||||||||||
Medical condition: PREDIABETES | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001327-41 | Sponsor Protocol Number: IMIB-RMV-2021-02 | Start Date*: 2021-07-12 |
Sponsor Name:Fundación para la formación e investigación sanitarias de la Región de Murcia | ||
Full Title: Withdrawal of pharmacological treatment in patients responding to cardiac resynchronization therapy: Open and randomized study | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003745-14 | Sponsor Protocol Number: D1448C00005 | Start Date*: 2006-01-13 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Multi-centre, Double-blind, Randomised Withdrawal, Parallel-group, Placebo-controlled Phase III Study of the Efficacy and Safety of Quetiapine Fumarate Sustained Release (Seroquel SR®) as Monothe... | ||
Medical condition: Maintenance treatment of patients with Major Depressive Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) FI (Completed) SK (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000206-36 | Sponsor Protocol Number: DOPA1 | Start Date*: 2014-10-27 |
Sponsor Name: | ||
Full Title: DRD4 genotype as a moderator of L-Dopa intervention effects on parent-related neurocognitive processes, behaviors, and attitudes: A micro-trial of differential susceptibility to pharmacological int... | ||
Medical condition: There are no medical conditions or diseases under investigation. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002372-36 | Sponsor Protocol Number: 2022-16039 | Start Date*: 2024-01-02 |
Sponsor Name:Wageningen Research Stichting | ||
Full Title: The CanISleepinMS Study: Effect of cannabidiol (CBD) on sleep quality in patients with multiple sclerosis, a series of 15 randomised, placebo controlled N-of-1 trials | ||
Medical condition: Insomnia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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