- Trials with a EudraCT protocol (2,395)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
2,395 result(s) found for: Day hospital.
Displaying page 1 of 120.
| EudraCT Number: 2016-003557-15 | Sponsor Protocol Number: HMB-ICU | Start Date*: 2018-08-31 | |||||||||||
| Sponsor Name:Guy's and St Thomas NHS Foundation Trust | |||||||||||||
| Full Title: A Study to Investigate the Effect of β-Hydroxy-β-Methylbutyrate (HMB) on Skeletal Muscle Wasting in Early Critical Illness. | |||||||||||||
| Medical condition: Critical illness | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003489-28 | Sponsor Protocol Number: VITDCUT | Start Date*: 2018-02-19 |
| Sponsor Name:Medizinische Universität Graz | ||
| Full Title: Influence of high dose vitamin D3 intake on outcome in pancreatic cancer surgery: prospective, randomized, open, controlled study | ||
| Medical condition: vitamin D deficiency - pancreatic cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005596-90 | Sponsor Protocol Number: NL51548.100.14 | Start Date*: 2015-04-22 |
| Sponsor Name:St. Lucas Andreas Hospital | ||
| Full Title: Comparison of femoral nerve block with posterior capsule infiltration versus anterior and posterior capsule infiltration after total knee replacement. | ||
| Medical condition: patienst requiring total knee replacement for non-inflammatory osteoarthritis of the knee | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002251-13 | Sponsor Protocol Number: 24052016 | Start Date*: 2016-11-09 |
| Sponsor Name:Oulu university hospital | ||
| Full Title: The effect of intravenous single-dose dexamethasone on pain after total knee replacement surgery. | ||
| Medical condition: Patients with arthrosis of knee joint needing operative treatment i.e. arthroplasty of knee. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-001051-12 | Sponsor Protocol Number: 11RM013 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Nottingham University Hospitals NHS Trust | |||||||||||||
| Full Title: Early low dose steroids for adults admitted to hospital with influenza-like illness during a pandemic: a randomised placebo controlled trial | |||||||||||||
| Medical condition: Influenza-like illness | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000887-23 | Sponsor Protocol Number: CTIN816B12201 | Start Date*: 2022-10-03 | ||||||||||||||||
| Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||
| Full Title: A multicenter, participant and investigator-blinded, randomized, placebo-controlled Phase 2a study to investigate the pharmacokinetics, pharmacodynamics, safety and tolerability of TIN816 in the tr... | ||||||||||||||||||
| Medical condition: Acute kidney injury Due to sepsis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Restarted) FR (Completed) DE (Completed) BE (Completed) HU (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-003661-19 | Sponsor Protocol Number: 006 | Start Date*: 2020-10-27 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Beta-blockade with landiolol in out-of-hospital cardiac arrest: a randomized, double-blind, placebo-controlled, pilot trial | ||
| Medical condition: out-of-hospital cardiac arrest | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002636-31 | Sponsor Protocol Number: APHP211034 | Start Date*: 2022-09-15 |
| Sponsor Name:Assistance Publique Hôpitaux de Paris/DRCI | ||
| Full Title: Piperacillin-tazobactam and temocillin as carbapenem-alternatives for the treatment of severe infections due to extended-spectrum beta-lactamase–producing Gram-negative Enterobacteriaceae in the in... | ||
| Medical condition: severe infections due to extended-spectrum beta-lactamase–producing Gram-negative Enterobacteriaceae | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004248-11 | Sponsor Protocol Number: Ahus-ATHENIAN | Start Date*: 2021-11-10 |
| Sponsor Name:Akershus University Hospital | ||
| Full Title: Antibiotic THErapy iN vIral Airway iNfections (ATHENIAN): An open labelled randomized controlled pragmatic trial to evaluate the efficacy and safety of discontinuing antibiotic therapy in adult pat... | ||
| Medical condition: Patients with viral respiratory tract infection (influenza virus, parainfluenza virus, respiratory syncytial virus or human metapneumovirus) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002801-23 | Sponsor Protocol Number: Metamizole002 | Start Date*: 2019-10-08 |
| Sponsor Name:Jessa Hospital | ||
| Full Title: Evaluation of the added value of Metamizole to standard post-operative treatment after ambulant surgery: a double-blind, randomized controlled trial | ||
| Medical condition: Optimalization of post-operative treatment after ambulant surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001203-16 | Sponsor Protocol Number: LIBERATE | Start Date*: 2020-05-06 | |||||||||||||||||||||
| Sponsor Name:Guy's and St Thomas' NHS Foundation Trust [...] | |||||||||||||||||||||||
| Full Title: Lipid ibuprofen versus standard of care for acute hypoxaemic respiratory failure due to COVID-19: a multicentre, randomised, controlled trial | |||||||||||||||||||||||
| Medical condition: COVID-19; respiratory failure; hypoxaemia. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2019-000839-21 | Sponsor Protocol Number: DREPADOL | Start Date*: 2019-06-17 | |||||||||||
| Sponsor Name:Centre Hospitalier Intercommunal de Créteil | |||||||||||||
| Full Title: Evaluation of the efficacy and safety of aprepitant in the management of vaso-occlusive crisis in sickle cell children: randomized, single-center, randomized, phase IIb/III prospective study | |||||||||||||
| Medical condition: vaso-occlusive crisis for patients with sickle cell disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Not Authorised) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001616-18 | Sponsor Protocol Number: TACTIC-COVID | Start Date*: 2020-04-18 | |||||||||||
| Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Treatment with inhaled corticoids in patients with COVID-19 admitted to hospital with pneumonia | |||||||||||||
| Medical condition: COVID19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004406-10 | Sponsor Protocol Number: 000 | Start Date*: 2013-10-09 |
| Sponsor Name:University Hospital Hradec Kralove | ||
| Full Title: The use of oxygen and hydrogen mixture for inhalation to prevent ischaemia-reperfusion injury | ||
| Medical condition: The patients suffering form acute transmural myocardial infarction and treated with percutaneous transluminal coronary angioplasty will be included in the study. After the recanalisation of occlude... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006951-32 | Sponsor Protocol Number: REP0321 | Start Date*: 2022-04-05 | |||||||||||
| Sponsor Name:Dompé farmaceutici s.p.a. | |||||||||||||
| Full Title: Reparixin 1200 mg three times a day as add-on therapy to standard of care to limit disease progression in hospitalised adult patients with COVID-19 and other community-acquired pneumonia. A multina... | |||||||||||||
| Medical condition: COVID-19 and other community-acquired pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) IT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001200-42 | Sponsor Protocol Number: CamoCO-19-001 | Start Date*: 2020-03-30 | |||||||||||
| Sponsor Name:Department of Infecitous Diseases, Aarhus University Hospital | |||||||||||||
| Full Title: The Impact of Camostat Mesilate on COVID-19 Infection: An investigator-initiated randomized, placebo-controlled, phase IIa trial | |||||||||||||
| Medical condition: 2019-nCoV acute respiratory disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001285-15 | Sponsor Protocol Number: KOIIM-2019-1 | Start Date*: 2019-06-28 |
| Sponsor Name:University Medical Centre Ljubljana | ||
| Full Title: Platelet inhibition with cangrelor in comatose survivors of out-of-hospital cardiac arrest undergoing primary percutaneous coronary intervention | ||
| Medical condition: Comatose survivors of out-of-hospital cardiac arrest undergoing primary percutaneous coronary intervention | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000890-25 | Sponsor Protocol Number: 202002102 | Start Date*: 2020-03-05 |
| Sponsor Name:Fondation Méditerranée Infection (FMI) - IHU Méditerranée Infection | ||
| Full Title: Treatment of Coronavirus SARS-Cov2 Respiratory Infections with Hydroxychloroquine | ||
| Medical condition: Patients with documented respiratory infection with coronavirus SARS COV 2 | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003820-22 | Sponsor Protocol Number: 2016-Longterm-OX | Start Date*: 2016-12-22 | |||||||||||
| Sponsor Name:Dutch Growth Research Foundation | |||||||||||||
| Full Title: Intranasal administration of oxytocin in children with Prader-Willi Syndrome. A randomized, open-label, cross-over trial of different treatment regimens of oxytocin administration. Effects on eatin... | |||||||||||||
| Medical condition: Prader-Willi syndrome | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Not Authorised) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004237-21 | Sponsor Protocol Number: Metamizole003 | Start Date*: 2020-11-27 |
| Sponsor Name:Jessa Hospital | ||
| Full Title: Evaluation of the added value of Metamizole to standard postoperative treatment after ambulant shoulder surgery: a double-blind, randomized controlled trial | ||
| Medical condition: Optimalisation of postoperative treatment after ambulant shoulder arthroscopy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
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