- Trials with a EudraCT protocol (2,833)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
2,833 result(s) found for: Classification.
Displaying page 1 of 142.
EudraCT Number: 2015-005220-26 | Sponsor Protocol Number: ACE-LY-308 | Start Date*: 2017-05-16 | |||||||||||
Sponsor Name:Acerta Pharma BV | |||||||||||||
Full Title: A Phase 3, Randomized, Double blind, Placebo controlled, Multicenter Study of Bendamustine and Rituximab (BR) alone Versus in Combination with Acalabrutinib (ACP 196) in Subjects with Previously Un... | |||||||||||||
Medical condition: Mantle Cell Lymphoma | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Ongoing) DE (Ongoing) BE (Ongoing) ES (Ongoing) CZ (Ongoing) GR (Ongoing) PL (Ongoing) FR (Ongoing) IT (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000070-29 | Sponsor Protocol Number: 74668 | Start Date*: 2022-09-15 |
Sponsor Name:VU University Medical Center | ||
Full Title: A Proof-of-Concept Study to Explore the Potential Efficacy of Deferiprone in Patients With Pelizaeus-Merzbacher disease (PMD) | ||
Medical condition: Pelizaeus-Merzbacher disease | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001409-21 | Sponsor Protocol Number: IMIB-DFC-2020-02 | Start Date*: 2020-04-01 |
Sponsor Name:FFIS | ||
Full Title: A prospective, multicenter, randomized, parallel, double-blind, placebo-controlled phase IIb clinical trial to evaluate intravenous infusion of Defibrotide in the prevention and treatment of respir... | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000212-16 | Sponsor Protocol Number: HYKS-190116 | Start Date*: 2016-04-12 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Hydrocortisone vs. pasireotide in preventing pancreatic fistula and other complications after pancreatic resection - a prospective, randomized, controlled trial | ||
Medical condition: Patients undergoing pancreatic resection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001818-16 | Sponsor Protocol Number: LT-CLL-001 | Start Date*: 2007-07-05 | ||||||||||||||||
Sponsor Name:Vilnius University Hospital Santariskiu Clinics | ||||||||||||||||||
Full Title: Phase II Study of High-dose Methylprednisolone and Rituximab in Previously Treated Patients with High Risk Chronic B Lymphocytic Leukemia | ||||||||||||||||||
Medical condition: Treated high-risk chronic B lymphocytic leukemia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001284-24 | Sponsor Protocol Number: BGB-3111-214 | Start Date*: 2019-04-01 | |||||||||||
Sponsor Name:BeiGene, Ltd. | |||||||||||||
Full Title: A Phase 2, Open-label Study of Zanubrutinib (BGB-3111) in Patients with Relapsed or Refractory Marginal Zone Lymphoma | |||||||||||||
Medical condition: Relapsed or Refractory Marginal Zone Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001438-25 | Sponsor Protocol Number: VWM1 | Start Date*: 2020-04-21 |
Sponsor Name:VU University Medical Center | ||
Full Title: A Study to Explore the Safety, Tolerability, Pharmacokinetic Profile, and Potential Efficacy of Guanabenz in Patients With Early Childhood Onset Vanishing White Matter (VWM) | ||
Medical condition: Vanishing white matter | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003132-23 | Sponsor Protocol Number: 41354 | Start Date*: 2012-11-27 |
Sponsor Name: | ||
Full Title: Local tumescent anaesthesia with ambulatory phlebectomy according to Muller | ||
Medical condition: Varices according to the CEAP classification | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003586-45 | Sponsor Protocol Number: Painscales_Sedation_1 | Start Date*: 2009-09-24 |
Sponsor Name:Department of Anaesthesie, General Intensive Care and Pain Therapy | ||
Full Title: The precision of three pain scales as a function of sedation | ||
Medical condition: This is a patient study in patients with a planned operation under general anaesthesie including healthy or merately ill patients (anaesthesia risk classification ASA 1-3). Pain self assessment as ... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002730-16 | Sponsor Protocol Number: GLS27-005 | Start Date*: 2021-10-25 | |||||||||||
Sponsor Name:GeneOne Life Science Inc. | |||||||||||||
Full Title: Safety, Tolerability, Efficacy and Dose Response of GLS-1027 in the Prevention of Severe Pneumonitis caused by SARS-CoV-2 Infection | |||||||||||||
Medical condition: Patients with SARS-CoV-2 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002139-41 | Sponsor Protocol Number: R1979-ONC-1625 | Start Date*: 2019-08-14 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: An Open-Label Study to Assess the Anti-Tumor Activity and Safety of REGN1979, an anti CD20 x anti-CD3 Bispecific Antibody, in Patients with Relapsed or Refractory B-cell non-Hodgkin Lymphoma | |||||||||||||
Medical condition: Relapsed/refractory B-cell non-Hodgkin lymphoma (NHL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Ongoing) DE (Ongoing) ES (Temporarily Halted) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001777-86 | Sponsor Protocol Number: 91710346.1.2 | Start Date*: 2012-10-23 |
Sponsor Name: | ||
Full Title: Pilot study for classification of attempted movement from the electroencephalogram in healthy participants with a temporary paralysis of one arm induced by local administration of rocuronium | ||
Medical condition: Intraoperative awareness during general anesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002579-33 | Sponsor Protocol Number: EE-301 | Start Date*: 2020-03-26 | |||||||||||
Sponsor Name:Phathom Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Two-Phase, Multicenter Study to Evaluate the Efficacy and Safety of Vonoprazan 20 mg Compared to Lansoprazole 30 mg for Healing in Patients with Erosive Esophag... | |||||||||||||
Medical condition: Erosive Esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) HU (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004951-55 | Sponsor Protocol Number: E2090-AS086-311 | Start Date*: 2017-04-24 |
Sponsor Name:Eisai Inc. | ||
Full Title: A Multicenter, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of Zonisamide in the Treatment of Partial Seizures | ||
Medical condition: Epilepsy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2019-003699-38 | Sponsor Protocol Number: CEDM-MRI | Start Date*: 2021-04-28 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | |||||||||||||
Full Title: DETECTION RATE AND CLASSIFICATION OF BREAST LESIONS WITH DIGITAL MAMMOGRAPHY WITH CONTRAST MEDIUM (CEDM) ALONE AND IN COMBINATION WITH TOMOSYNTHESIS COMPARED TO MR IMAGING WITH GADOLINIUM IN DYNAMI... | |||||||||||||
Medical condition: Breast souspicious lesions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003783-30 | Sponsor Protocol Number: EME-163-LOR-0025-I | Start Date*: 2005-04-27 |
Sponsor Name:Technical Unversity of Munich | ||
Full Title: Application of Aprepitant as salvage prophylaxis after failure of a conventional antiemetic therapy during moderately emetogenic chemotherapy in gastrointestinal cancer | ||
Medical condition: Chemotherapy-induced nasuea and vomiting (CINV) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-003543-67 | Sponsor Protocol Number: 2007-285-31-3 | Start Date*: 2007-10-30 |
Sponsor Name:Karolinska Universitetssjukhuset | ||
Full Title: Assessment of bronchial hyperresponsiveness in children - inhalation of Mannitol compared to eucapnic voluntary hyperventilation and methacholine provocation | ||
Medical condition: Three different methods to assess airway hyperresponsiveness in children with allergic asthma will be compared. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000210-21 | Sponsor Protocol Number: TON/02/05-CLIN | Start Date*: 2006-03-27 |
Sponsor Name:Prof Jes Olesen | ||
Full Title: A single centre, double-blind, randomised, placebo controlled cross-over study to evaluate the efficacy and tolerability of tonabersat in the prophylaxis of migraine in patients presenting with mig... | ||
Medical condition: Migraine with aura meeting the diagnostic criteria of the International Classification of Headache Disorders (Edition 2) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004582-14 | Sponsor Protocol Number: XENOMICRO | Start Date*: 2014-01-28 |
Sponsor Name:Department of Anesthesiology and Perioperative Medicine | ||
Full Title: Haemodynamic effects of xenon or sevoflurane anesthesia on microcirculation | ||
Medical condition: Patients with ASA III classification (left ventricular failure) undergoing implantation of a defibrillator. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000547-28 | Sponsor Protocol Number: 070774 | Start Date*: 2006-01-15 |
Sponsor Name:Department of Psychiatry; Section of Sleep Research and Pharmacopsychiatry | ||
Full Title: EEG and ERP tomography by means of LORETA (Low-Resolution Brain Electromagnetic Tomography) identifying essential brain regions for vigilance and cognition in narcolepsy: double-blind, placebo-cont... | ||
Medical condition: Patients complaining of excessive daytime sleepiness will be recruited from our sleep clinics and will be subjected to neuropsychiatric, physical, laboratory and neurophysiological screening examin... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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