- Trials with a EudraCT protocol (1,346)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (202)
1,346 result(s) found for: Medicine.
Displaying page 1 of 68.
EudraCT Number: 2012-004082-41 | Sponsor Protocol Number: DELIcu | Start Date*: 2013-03-06 | |||||||||||
Sponsor Name:Dekan of Faculty of Medicine of Goethe-University Frankfurt | |||||||||||||
Full Title: Monocenter, double blind, randomised, placebo controlled study t evaluate Physostigmin for the Treatment of delirium in perioperative intensive care medicine | |||||||||||||
Medical condition: patients with delirium in perioperative intensive care medicine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004463-39 | Sponsor Protocol Number: 221921 | Start Date*: 2019-03-06 |
Sponsor Name:Sahlgrenska University Hospital, Department of Internal Medicine/Respiratory Medicine and Allergology [...] | ||
Full Title: Influence on cough and airway symptoms by oral capsaicin (capscium oleoresin ) – a phase II, randomised, placebo-controlled clinical study in patients with chronic idiopathic cough | ||
Medical condition: Chronic idiopathic cough | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000556-11 | Sponsor Protocol Number: RAPID_01 | Start Date*: 2022-04-26 |
Sponsor Name:Medical University of Vienna, Department of Anesthesia, Intensive Care Medicine and Pain Medicine | ||
Full Title: The effect of desflurane versus Sevoflurane on postoperative recovery in patients undergoing minor- to moderate-risk noncardiac surgery - a prospective double-blinded randomized clinical trial | ||
Medical condition: The evaluation of recovery times between desflurane and sevoflurane general anesthesia in patients ≥ 65 years of age undergoing minor- to moderate-risk noncardiac surgery | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005522-22 | Sponsor Protocol Number: Rifa-BP | Start Date*: 2012-01-23 |
Sponsor Name:Oulu University Hospital, Department of Internal Medicine | ||
Full Title: The effects of PXR activation on blood pressure regulation | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017458-11 | Sponsor Protocol Number: DEP-HOM | Start Date*: 2010-06-10 |
Sponsor Name:Institute for Social Medicine, Epidemiology, and Health Economics, Charité Berlin | ||
Full Title: Homeopathy for Depression: a randomized, four-armed, partial double-blind study. | ||
Medical condition: F32.1 Moderate Depressive Episode | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-000317-22 | Sponsor Protocol Number: BRE-ASA01 | Start Date*: 2017-04-13 |
Sponsor Name:Linköping University | ||
Full Title: A pilot study of low dose acetylsalicylic acid (ASA) for reduction of breast density and inflammation | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005215-42 | Sponsor Protocol Number: KloMid02 | Start Date*: 2013-04-12 |
Sponsor Name:Department of Anesthesiology and Intensive Care Medicine | ||
Full Title: Children's mood/anxiety, pain, nausea and behavioral changes after premedication with Clonidine versus Midazolam in ENT day surgery. | ||
Medical condition: Preanesthetic Medication at ear-nose-throat surgery | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002137-32 | Sponsor Protocol Number: FV001 | Start Date*: 2017-09-05 |
Sponsor Name:Hans-Gustaf Ljunggren | ||
Full Title: Immunological responses after concomitant vaccination with the yellow fever-vaccine Stamaril and the TBE-vaccine FSME Immun, or JE-vaccine Ixiaro | ||
Medical condition: Prevention of TBE or Japanece encephalitis by co-vaccination with the yellow fever vaccine | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-012297-12 | Sponsor Protocol Number: 920134 | Start Date*: 2009-08-12 |
Sponsor Name:Bioforce AG | ||
Full Title: Safety and Efficacy of long-term treatment with Echinaforce® over 4 months | ||
Medical condition: common cold | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2006-005175-18 | Sponsor Protocol Number: 151610/06 | Start Date*: 2007-09-27 |
Sponsor Name:Dpt. of Internal Medicine, Medical University of Innsbruck | ||
Full Title: Influence of insulin Levemir on endothelial function in type 2 diabetes mellitus. A prospective case-control study. | ||
Medical condition: Patients with known history of type 2 Diabetes Mellitus longer than 6 months, who were treated by diet in combination with oral antidiabetic drugs (OADs) are to be included in the study. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-004106-87 | Sponsor Protocol Number: CAS CVVH | Start Date*: 2007-10-23 |
Sponsor Name:Meical University, Dpt. Internal Medicine, Div. of General Internal Medicine | ||
Full Title: CLINICAL PHARMACOKINETICS OF CASPOFUNGIN IN CRITICALLY ILL PATIENTS DURING CONTINUOUS VENO-VENOUS HEMOFILTRATION | ||
Medical condition: Plasma concentrations of Caspofungin will be measured in patients requiring treatment with Cancidas (Caspofungin) and continuous veno-venous hemofiltration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004244-35 | Sponsor Protocol Number: 1/25-03-2014 | Start Date*: 2015-03-05 | |||||||||||
Sponsor Name:IRCCS Ospedale San Raffaele | |||||||||||||
Full Title: AMYLOID LOAD IN PRODROMAL AD WITH LIMBIC-PREDOMINANT PHENOTYPE PRINCIPAL INVESTIGATOR - STUDIO DEL CARICO DI AMILOIDE IN AD PRODROMICO CON FENOTIPO LIMBICO | |||||||||||||
Medical condition: mild cognitive impairment, Alzheimer's disease prodromal | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001211-13 | Sponsor Protocol Number: PRODROMALAD | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: IMAGING OF NEUROINFLAMMATION AND NEURODEGENERATION IN ALZHEIMER’S DISEASE | |||||||||||||
Medical condition: mild cognitive impairment and familiar Alzheimer disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003669-24 | Sponsor Protocol Number: NET-2011-02346784 | Start Date*: 2017-01-30 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: Amyloid PET imaging study for the diagnosis of Alzheimer's disease in the preclinical/predementia phase | |||||||||||||
Medical condition: memory complaint, mild cognitive impairment, Alzheimer's Disease in predrmentia/prodromal disease phases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004107-20 | Sponsor Protocol Number: CAS ELF | Start Date*: 2007-10-23 |
Sponsor Name:Medical University, Dpt. Internal Medicine, Div. of General Internal Medicine | ||
Full Title: LUNG PENETRATION OF CASPOFUNGIN INTO EPITHELIAL LINING FLUID | ||
Medical condition: Plasma and ELF concentrations of Caspofungin will be measured in patients requiring treatment with Cancidas (Caspofungin) for fungal infection (proven or suspected) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023120-24 | Sponsor Protocol Number: Nitro1 | Start Date*: 2011-10-18 | |||||||||||
Sponsor Name:MAASTRO clinic | |||||||||||||
Full Title: Nitroglycerin's effect on perfusion and hypoxia in human non small cell lung cancer: proof of principle, a phase II trial | |||||||||||||
Medical condition: non small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003645-10 | Sponsor Protocol Number: 2014-LSB | Start Date*: 2014-11-27 |
Sponsor Name:Department of Endocrinology and Internal Medicine | ||
Full Title: Physiological interactions between the adrenal- and the parathyroid glands described by controlled clinical trials | ||
Medical condition: Secondary hyperparathyrodism due to Vitamin D deficiency | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003842-27 | Sponsor Protocol Number: Studio-flourochinoloni-in-BPCO. | Start Date*: 2008-10-14 |
Sponsor Name:CENTRO STUDI FADOI | ||
Full Title: Randomized, single-blind, parallel groups, controlled study to compare levofloxacin and prulifloxacin in patients with exacerbations of COPD previously treated with different antibiotics and admitt... | ||
Medical condition: - Patients with acute exacerbation of COPD of possible infectious origin, previously treated with antibiotic therapy (no quinolones), without clinical improvement, and hospitalized in Internal Medi... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
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: 2017-000414-35 | Sponsor Protocol Number: AITT2016/2 | Start Date*: 2017-04-21 | |||||||||||
Sponsor Name:University of Debrecen Faculty of Medicine, Department of | |||||||||||||
Full Title: Administration of Preemptive Analgesia by Dexketoprofen to prevent Acute and Chronic Postcraniotomy Headache. A randomized Placebo Controlled, Single-center Study | |||||||||||||
Medical condition: Headache | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Ongoing) | |||||||||||||
Trial results: (No results available) |
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