- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25 result(s) found for: .uci.
Displaying page 1 of 2.
EudraCT Number: 2009-017353-36 | Sponsor Protocol Number: GlnHSD-001-09 | Start Date*: 2010-06-17 |
Sponsor Name:Jon Perez Barcena | ||
Full Title: Eficacia del dipéptido N(2)-L-Alanil-L-glutamina en los pacientes traumáticos ingresados en la UCI: estudio piloto, prospectivo, aleatorizado y doble ciego | ||
Medical condition: PPacientes traumáticos ingresados en UCI que cumplan los criterios: - Edad igual o superior a 18 años; - Injury Severity Score superior a 10 puntos; - Pacientes que requieran nutrición enteral o ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001671-36 | Sponsor Protocol Number: EC11-103 | Start Date*: 2012-08-27 |
Sponsor Name:Fundación para la Investigación Biomédica | ||
Full Title: A phase IV randomized, controlled clinical trial to compare the high flow oxygen therapy (group of intervention) opposite to the conventional oxygen therapy (group control) in patients with severe ... | ||
Medical condition: Severe acute respiratory failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022901-16 | Sponsor Protocol Number: TRAMA | Start Date*: 2011-07-28 | ||||||||||||||||
Sponsor Name:Gemma Rialp | ||||||||||||||||||
Full Title: Estudio multicéntrico sobre el efecto del tratamiento de la alcalosis metabólica con acetazolamida en la duración de la ventilación mecánica. | ||||||||||||||||||
Medical condition: Enfermedad pulmonar obstructiva crónica y síndrome de obesidad ventilación | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001299-38 | Sponsor Protocol Number: EMULIP | Start Date*: 2004-11-26 |
Sponsor Name:Metabolism and Nutrition Group of the SEMICYUC | ||
Full Title: Study prospective, multicenter, randomized, comparative, double blind, to evaluate two different lipidic emulsions in the total parenteral nutrition of the critic patient and their influence in the... | ||
Medical condition: Patients in whom the necessity is foreseen to receive metabolic total parenteral nutrition like nutritional support, during a minimum period of 7 days, because they can not to be fed by route enter... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001333-13 | Sponsor Protocol Number: 20-37815010 | Start Date*: 2020-04-09 |
Sponsor Name:Groupe Hospitalier Paris Saint-Joseph | ||
Full Title: Dexamethasone associated with hydroxychloroquine vs. hydroxychloroquine alone for the early treatment of severe ARDS caused by COVID-19 : a randomized controlled trial | ||
Medical condition: Acute Respiratory Distress Syndrome (ARDS) caused by SARS-Cov-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018716-33 | Sponsor Protocol Number: PHRN09-AM/MUCIS | Start Date*: 2010-10-21 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Etude de l'efficacité du méthotrexate en adjonction d'un anti-histaminique H1 dans le traitement de l'urticaire chronique idiopathique sévère réfractaire aux anti-H1 seuls : essai randomisé. | |||||||||||||
Medical condition: urticaire chronique idiopathique sévère | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001929-31 | Sponsor Protocol Number: ESCORPIO | Start Date*: 2020-06-16 |
Sponsor Name:Fundación Investigación Biomédica Hospital Ramón y Cajal | ||
Full Title: Controlled, randomized, non-blind trial on the usefulness of pioglitazone treatment in patients with type 2 diabetes mellitus and COVID-19. | ||
Medical condition: COVID-19 in patients with diabetes mellitus type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002434-33 | Sponsor Protocol Number: Aprotinin1.0. | Start Date*: 2020-10-16 |
Sponsor Name:Hospital General Universitario Ciudad Real | ||
Full Title: Phase 3 randomized study to evaluate the safety and efficacy of aprotinin (Trasylol®) administered by inhalation nebulization in patients diagnosed with SARS-CoV-2 (COVID-19) with moderate severity... | ||
Medical condition: Patients with moderate SARS-CoV-2 pneumonia confirmed with a diagnosis of polymerase chain reaction (PCR) before randomization. The patient should be hospitalized and require ongoing medical care f... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005951-16 | Sponsor Protocol Number: UCI-01 | Start Date*: 2006-07-07 |
Sponsor Name:Dr. Joan Ramon Masclans. Servicio de Medicina Intensiva. Hospital Universitario Vall d'Hebron | ||
Full Title: Ensayo clínico piloto, aleatorizado, controlado con placebo, paralelo, doble ciego, para evaluar el efecto de salbutamol intravenoso sobre marcadores de inflamación en pacientes con síndrome de dis... | ||
Medical condition: Síndrome de distrés respiratorio agudo | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-000756-41 | Sponsor Protocol Number: DEB-EPIV-201 | Start Date*: 2006-04-24 |
Sponsor Name:Debiopharm SA | ||
Full Title: Phase IIa Multicenter 1 Week Treatment, Randomised, Double-Blind, Placebo Controlled Study of Depelestat in Patients Suffering from Acute Respiratory Distress Syndrome | ||
Medical condition: Acute Respiratory Distress Syndrome (ARDS) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005948-24 | Sponsor Protocol Number: UVIR-90390 | Start Date*: 2008-02-01 | |||||||||||
Sponsor Name:Dr. Miguel Ferrer. Servicio de Neumología. Hospital Clínic de Barcelona | |||||||||||||
Full Title: Eficacia de los glucocorticoides en la neumonía asociada a la ventilación mecánica. Ensayo clínico aleatorizado, enmascarado a doble ciego y controlado con placebo. | |||||||||||||
Medical condition: Neumonía asociada a ventilación mecánica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001319-71 | Sponsor Protocol Number: F1K-MC-EVBQ | Start Date*: 2004-08-13 |
Sponsor Name:Lilly S.A. | ||
Full Title: A Phase IIIb Study to Determine Efficacy and Safety of Extended Drotrecogin Alfa (Activated) Therapy in Patients With Persistent Requirement for Vasopressor Support After 96-Hour Infusion With Comm... | ||
Medical condition: in severe sepsis patients with persistent vasopressordependent hypotension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003542-33 | Sponsor Protocol Number: HC – G – H – 0510 | Start Date*: 2006-06-05 |
Sponsor Name:B Braun Medical S.A. | ||
Full Title: Estudio prospectivo, multicéntrico, aleatorizado, comparativo, doble ciego, para evaluar dos emulsiones lipídicas diferentes en la nutrición parenteral total del enfermo crítico y su influencia en ... | ||
Medical condition: Pacientes en los que se prevea la necesidad de recibir nutrición parenteral total como soporte metabólico nutricional, durante un período mínimo de 5 días, al no poder ser alimentados por vía enter... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005047-42 | Sponsor Protocol Number: REOX | Start Date*: 2009-04-07 | |||||||||||
Sponsor Name:Máximo Vento Torres | |||||||||||||
Full Title: REANIMACIÓN DEL RECIÉN NACIDO DE EXTREMADO BAJO PESO MEDIANTE UN SISTEMA DE MONITORIZACIÓN INTEGRAL: ESTUDIO DE LA INFLUENCIA DE LA FRACCIÓN INSPIRATORIA DE OXÍGENO Resuscitation of very low birth... | |||||||||||||
Medical condition: Reducir la tasa de intubación en el paritorio derivada del establecimiento más rápido del movimiento diafragmático normal y de un patrón respiratorio fisiológico utilizando bajas concentraciones de... | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003828-36 | Sponsor Protocol Number: B22CS | Start Date*: 2015-10-22 | |||||||||||
Sponsor Name:Advicenne Pharma | |||||||||||||
Full Title: A multicentre, open-label, extension study, evaluating the safety and tolerability and the efficacy of ADV7103 at long term in distal renal tubular acidosis patients. | |||||||||||||
Medical condition: Distal renal tubular acidosis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004642-14 | Sponsor Protocol Number: 20050100 | Start Date*: 2006-01-30 |
Sponsor Name:Amgen S.A. | ||
Full Title: Estudio abierto, de un solo grupo, de palifermin para la reducción de la mucositis en sujetos con linfoma no Hodgkin (LNH) o mieloma múltiple (MM) sometidos a quimioterapia a altas dosis y trasplan... | ||
Medical condition: Mucositis Oral Oral Mucositis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006409-18 | Sponsor Protocol Number: 9463-EC-0002 | Start Date*: 2010-02-09 | ||||||||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | ||||||||||||||||||
Full Title: An Exploratory Study to Compare the Efficacy and Safety of Micafungin as a Pre-emptive Treatment of Invasive Candidiasis versus Placebo in High Risk Surgical Subjects - A Multicentre, Randomized, D... | ||||||||||||||||||
Medical condition: Invasive Candidiasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) ES (Completed) HU (Completed) BE (Completed) GR (Completed) DE (Completed) FR (Completed) FI (Completed) IT (Completed) GB (Completed) DK (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000837-39 | Sponsor Protocol Number: CCD01 | Start Date*: 2007-08-15 | |||||||||||
Sponsor Name:Cytonet GmbH & Co. KG | |||||||||||||
Full Title: Open, randomized, prospective, controlled, multicentre study to evaluate the efficacy and safety of multiple intraportal applications of liver cell suspension in patients with acute liver failure n... | |||||||||||||
Medical condition: Acute Liver Failure Subgroups of patients with indications falling under ICD classification codes:K70.4, K71, K72, K75, K76, K77 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022380-35 | Sponsor Protocol Number: 982 | Start Date*: 2011-06-10 | |||||||||||
Sponsor Name:Biotest AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, parallel-group, adaptive group-sequential phase II study, to determine the efficacy and safety of BT086 as an adjunctive treatment in ... | |||||||||||||
Medical condition: severe Community Acquired Pneumonia (sCAP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019760-36 | Sponsor Protocol Number: T05018-2004 | Start Date*: 2010-11-22 | |||||||||||
Sponsor Name:Grifols Therapeutics, Incorporated | |||||||||||||
Full Title: A Phase 2, Randomized, Open-label (with Blinded Plasminogen Activator and Placebo Control Groups) Study to Evaluate the Effects of Different Intra-thrombus Infusion Regimens of Plasmin (Human) Comp... | |||||||||||||
Medical condition: acute peripheral arterial occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Prematurely Ended) DE (Prematurely Ended) BE (Completed) ES (Prematurely Ended) CZ (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
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