- Trials with a EudraCT protocol (43,850)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
43,850 result(s) found.
Displaying page 1,786 of 2,193.
EudraCT Number: 2021-003716-12 | Sponsor Protocol Number: RHNIA-001-2021 | Start Date*: 2022-08-24 | ||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||
Full Title: S-ketamine for cortical spreading depolarisation in patients with severe acute brain injury | ||||||||||||||||||||||||||||
Medical condition: Severe acute brain injury caused by aneurysmal subarachnoid hemorrhage, spontaneous intracerebral hemorrhage or traumatic brain injury. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002028-19 | Sponsor Protocol Number: RH-CARD-Pharma001 | Start Date*: 2022-02-01 | |||||||||||
Sponsor Name:Department of Cardiology, Copenhagen University Hospital Rigshospitalet | |||||||||||||
Full Title: Low-dose dobutamine infusion and single-dose tocilizumab in acute myocardial infarction patients with high risk of cardiogenic shock development – a 2x2 multifactorial, double-blinded, randomized, ... | |||||||||||||
Medical condition: Acute Myocardial Infarction with increased risk of Cardiogenic Shock. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004996-14 | Sponsor Protocol Number: AK_2021_HP | Start Date*: 2022-04-18 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase IIa Clinical Trial: Feasibility Study on Non-Invasive Simultaneous Hyperpolarized [1-13C]Pyruvate Magnetic Resonance Spectroscopy and 18F-FDG PET (hyperPET) for Metabolic Imaging in Patients ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Breast cancer, neuroendocrine neoplasms | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003265-26 | Sponsor Protocol Number: 345 | Start Date*: 2017-01-03 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Pharmacokinetic/Pharmacodynamic effects of add-on antiplatelet therapy with parenteral cangrelor as compared to standard dual antiplatelet treatment in patients with ST-elevation myocardial infarct... | ||
Medical condition: ST-elevation myocardial infarction, cardiac arrest | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2016-001313-24 | Sponsor Protocol Number: SUPERADD | Start Date*: 2017-02-13 | ||||||||||||||||||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin | ||||||||||||||||||||||||||||
Full Title: SUbstition of PERioperative Albumin Deficiency Disorders | ||||||||||||||||||||||||||||
Medical condition: High risk surgical patients or procedures showing a hypoalbuminemia intraoperatively. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005014-30 | Sponsor Protocol Number: AlproECMO_1.0 | Start Date*: 2016-06-02 | ||||||||||||||||
Sponsor Name:Medical University of Vienna, Department of Internal medicine I | ||||||||||||||||||
Full Title: A prospective randomized, double blind study on safety and efficacy of Alprostadil as additional Anticoagulant in Patients with veno- venous ECMO | ||||||||||||||||||
Medical condition: pulmonary insufficiency, which cannot be treated with measures of mechanical ventilation alone, Conditions in which veno-venous extracorporeal membrane oxygenation therapy is indicated | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004537-25 | Sponsor Protocol Number: ET16-116 | Start Date*: 2017-11-06 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: An Phase II trial aiming to evaluate the clinical interest of ABEMACICLIB monotherapy in patients with locally advanced/metastatic head and neck cancer after failure of platinum and cetuximab or an... | |||||||||||||
Medical condition: Patients with locally advanced/metastatic head and neck cancer after failure of platinum and cetuximab or anti-EGFR-based | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003415-19 | Sponsor Protocol Number: JM-010CS03 | Start Date*: 2018-10-31 |
Sponsor Name:Contera Pharma | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study in Parkinson’s Disease Patients With Moderate to Severe Dyskinesia to Assess the Efficacy and Safety/Tolerability of Two Dose Co... | ||
Medical condition: Parkinson’s Disease Patients With Moderate to Severe Dyskinesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Restarted) IT (Ongoing) SK (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006991-18 | Sponsor Protocol Number: 2020/0423/HP | Start Date*: 2023-04-21 | |||||||||||
Sponsor Name:CHU de Rouen | |||||||||||||
Full Title: Postoperative anti-infective strategy following pancreaticoduodenectomy in patients with preoperative biliary stent | |||||||||||||
Medical condition: Patients with preoperative biliary stent treated by pancreaticoduodenectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002285-23 | Sponsor Protocol Number: POETIG | Start Date*: 2017-01-18 | |||||||||||
Sponsor Name:Universitaetsklinikum Essen | |||||||||||||
Full Title: Phase 2 trial of ponatinib in patients with metastatic and/or unresectable gastrointestinal stromal tumor (GIST) following failure or intolerance of prior therapy with imatinib (POETIG trial – POna... | |||||||||||||
Medical condition: gastrointestinal stromal tumor (GIST) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024202-34 | Sponsor Protocol Number: 24122010 | Start Date*: 2014-04-24 | |||||||||||
Sponsor Name:UNIVERSITÄTSMEDIZIN GÖTTINGEN, GEORG-AUGUST-UNIVERSITÄT,Klinik für Kinder- und Jugendpsychiatrie/Psychotherapie | |||||||||||||
Full Title: Effect of oxytocin on therapy results of a group based social skill training in adolescents with Autism Spectrum Disorder | |||||||||||||
Medical condition: high-functioning autismus spectrum disorders: autistic disorder (F84.0), Asperger syndrome (F84.5), atypical autism (F84.1) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003558-17 | Sponsor Protocol Number: TRx-237-039 | Start Date*: 2018-02-25 | |||||||||||
Sponsor Name:TauRx Therapeutics Ltd | |||||||||||||
Full Title: Randomized, Double-Blind, Placebo-Controlled, Three-Arm, 12-Month, Safety and Efficacy Study of Hydromethylthionine Mesylate (LMTM) Monotherapy in Subjects with Alzheimer's Disease Followed by a 12... | |||||||||||||
Medical condition: Alzheimer’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) PL (Completed) ES (Ongoing) FR (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000035-74 | Sponsor Protocol Number: 1.1_27.02.2023 | Start Date*: 2023-03-05 |
Sponsor Name:Medical University Vienna | ||
Full Title: Pharmacodynamics of Liposomal Bupivacaine for Peripheral Nerve Blockade: A Randomized, Triple-blinded, Cross Over Study in Volunteers | ||
Medical condition: To evaluate the pharmacodynamic effects of perineural administered liposomal bupivacaine on nerve block characteristics | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002481-32 | Sponsor Protocol Number: InflamAD | Start Date*: 2023-04-11 |
Sponsor Name:Amsterdam UMC VUmc | ||
Full Title: Imaging inflammation in Alzheimer's Disease | ||
Medical condition: Amyloid-beta positive individuals across the Alzheimer's disease continuum and amyloid-beta negative individuals without cognitive complaints | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001022-57 | Sponsor Protocol Number: Qutenza-FM-20 | Start Date*: 2020-12-18 | ||||||||||||||||
Sponsor Name:Wojciech Zbigniew Pawlak | ||||||||||||||||||
Full Title: The effect of Qutenza application in patients with post-operative neuropathic pain: A double-blind, randomized, controlled pilot study | ||||||||||||||||||
Medical condition: Post-operative neuropathic pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-006239-44 | Sponsor Protocol Number: NL37603.042.11 | Start Date*: 2012-10-02 |
Sponsor Name:Dutch Childhood Oncology Group | ||
Full Title: An international collaborative study to discontinue Imatinib/Glivec® in pediatric CML patients with sustained complete molecular response (STOPIMAPED) | ||
Medical condition: Chronic Myeloid Leukemia pediatric patients treated with Imatinib having achieved and maintained complete molecular remission for at least 2 years. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-001612-11 | Sponsor Protocol Number: 3005032 | Start Date*: 2018-01-11 | |||||||||||
Sponsor Name:Region Hovedstaden | |||||||||||||
Full Title: A COMPARISON OF DEXMEDETOMIDINE VS PLACEBO AFFECT ON SLEEP-QUALLITY IN MECHANICAL VENTILATED CRITICAL ILL PATIENTS | |||||||||||||
Medical condition: Sleeping problems in mechanical ventilated critical ill patients in ICU | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004278-40 | Sponsor Protocol Number: CA180-597 | Start Date*: 2015-11-09 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: Continuing Treatment for Subjects Who Have Participated on a Prior Protocol Investigating Dasatinib | ||
Medical condition: Newly Diagnosed Chronic Phase Philadelphia Chromosome Positive Chronic Myeloid Leukemia / Castration-Resistant Prostate Cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000148-76 | Sponsor Protocol Number: 3.0 | Start Date*: 2021-08-04 |
Sponsor Name:Stockholm Health Care Services | ||
Full Title: Effects of Montelukast on neuroinflammation in Parkinson's Disease. An open-label single-center trial. | ||
Medical condition: Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003866-19 | Sponsor Protocol Number: 83336 | Start Date*: 2023-05-01 |
Sponsor Name:Amsterdam UMC location AMC | ||
Full Title: The effect of low-dose rhythmic 17-β-estradiol administration on bone turnover in postmenopausal women | ||
Medical condition: Osteoporosis prevention | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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