- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
17 result(s) found for: Team nursing.
Displaying page 1 of 1.
EudraCT Number: 2006-001284-33 | Sponsor Protocol Number: ALS-3-06-P-401 | Start Date*: 2006-06-08 |
Sponsor Name:air liquide sante international | ||
Full Title: pain relief management by kalinox 170 bar for short-time painful procedure in paediatric patients "alivio del dolor con kalinox 170 bar en pacientes pediatricos sometidos a procedimientos doloroso... | ||
Medical condition: | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021789-31 | Sponsor Protocol Number: A3051139 | Start Date*: 2010-12-08 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 US | |||||||||||||
Full Title: A PHASE 4 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY EVALUATING THE EFFICACY AND SAFETY OF RE-TREATMENT WITH VARENICLINE IN SUBJECTS WHO ARE CURRENTLY SMOKING, AND WHO HAVE PRE... | |||||||||||||
Medical condition: Smoking Cessation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003138-17 | Sponsor Protocol Number: P1200_51 | Start Date*: 2020-01-17 | |||||||||||
Sponsor Name:Cliniques universitaires Saint-Luc | |||||||||||||
Full Title: A 24 weeks proof of concept study to evaluate the clinical, MRI and synovial tissue benefit of Sarilumab in active RA patients despite TNF agents | |||||||||||||
Medical condition: Medical condition – Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014916-37 | Sponsor Protocol Number: A3051122 | Start Date*: 2010-03-15 | |||||||||||
Sponsor Name:PFIZER | |||||||||||||
Full Title: "Estudio de fase 4, doble ciego, controlado con placebo, multicéntrico y de 12 semanas de duración para evaluar la seguridad y la eficacia del tartrato de Vareniclina (CP-526,555) 1 mg dos veces a... | |||||||||||||
Medical condition: "Dejar de Fumar" "Smoking cessation" | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001688-22 | Sponsor Protocol Number: 01CCRe-IV | Start Date*: 2013-08-23 | |||||||||||
Sponsor Name:Servicio de Cirugía General y Digestiva Hospital Universitario de Bellvitge | |||||||||||||
Full Title: Randomized multicenter trial in colorectal cancer patients with non-resectable metastasis. Impact of tumor resection versus chemotherapy alone in survival. | |||||||||||||
Medical condition: Cancer colorectal stage IV with synchronous non-resectable metastasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024181-22 | Sponsor Protocol Number: A0221095 | Start Date*: 2011-05-18 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A 12-WEEK, PHASE 4, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL GROUP, MULTICENTER TRIAL IN OVERACTIVE BLADDER SUBJECTS TO CONFIRM THE EFFICACY OF 8 MG FESOTERODINE COMPARED TO 4 MG F... | |||||||||||||
Medical condition: Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) HU (Completed) DE (Completed) FI (Completed) GR (Completed) LT (Completed) AT (Completed) DK (Completed) SK (Completed) BG (Prematurely Ended) NO (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002538-20 | Sponsor Protocol Number: EORTC 62027 | Start Date*: 2006-02-24 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Phase 2 study of Glivec (Imatinib) in locally advanced and/or metastatic soft tissue sarcomas expressing the t(17;22)(q22;q13) translocation resulting in a COL1A1/PDGF rearrangement i.e. DermatoFib... | |||||||||||||
Medical condition: Soft tissue sarcomas are a family of malignant diseases originating from mesenchymal cells. Two types of theses sarcomas, dermatofibrosarcoma protuberans (DFSP) and giant cell fibriblastoma(GCF), a... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003073-15 | Sponsor Protocol Number: 0504 | Start Date*: 2016-02-12 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Research Governance, University of Leicester | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: HYDration and bicarbonate to prevent acute Renal injury after endovascular Aneurysm repair: pilot-feasibility randomized controlled study (HYDRA pilot trial) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute kidney injury post endovascular repair of the abdominal aortic aneurysm. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-004277-27 | Sponsor Protocol Number: MT-1621-102 | Start Date*: 2019-07-16 |
Sponsor Name:Modis Therapeutics, Inc. | ||
Full Title: A Phase 2 open-label study of continuation treatment with combination pyrimidine nucleos(t)ides in patients with thymidine kinase 2 deficiency (TK2) | ||
Medical condition: Thymidine kinase 2 deficiency | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003543-30 | Sponsor Protocol Number: EORTC-1809-STBSG | Start Date*: 2020-12-16 | ||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | ||||||||||||||||||
Full Title: A randomized phase III study of neoadjuvant chemotherapy followed by surgery versus surgery alone for patients with High Risk RetroPeritoneal Sarcoma | ||||||||||||||||||
Medical condition: Primary high risk leiomyosarcoma or Liposarcoma of retroperitoneal space or infra-peritoneal spaces of pelvis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) SK (Trial now transitioned) PL (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) DE (Trial now transitioned) CY (Trial now transitioned) DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005249-51 | Sponsor Protocol Number: A7881013 | Start Date*: 2010-05-19 | |||||||||||
Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent UK | |||||||||||||
Full Title: A PHASE 2B, PARALLEL, DOUBLE BLIND, DOUBLE DUMMY, ACTIVE COMPARATOR AND PLACEBO CONTROLLED STUDY TO INVESTIGATE THE SAFETY, TOLERATION AND EFFICACY OF 6-WEEK QD ADMINISTRATION OF PF-00610355 CRC-74... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) ES (Completed) EE (Completed) BG (Completed) PL (Completed) DE (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000406-36 | Sponsor Protocol Number: EORTC-1707-GITCG | Start Date*: 2019-06-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | ||||||||||||||||||||||||||||||||||||||
Full Title: Adjuvant immunotherapy in patients with resected gastric cancer following preoperative chemotherapy with high risk for recurrence (N+ and/or R1): an open label randomized controlled phase-2-study (... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Gastric, lower esophageal or GE-junction adenocarcinoma | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) PL (Completed) NO (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023322-21 | Sponsor Protocol Number: NP031112-10B04 | Start Date*: 2011-04-13 | |||||||||||
Sponsor Name:Noscira S.A | |||||||||||||
Full Title: A multicenter, Randomized, Double-blind, Placebo-controlled, 4-arm, 26 week Parallel-Group Study to evaluate the Efficacy, Safety and Tolerability of Two Oral Doses and Two Regimes of Tideglusib vs... | |||||||||||||
Medical condition: Alzheimer's Disease (mild to moderate) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) FI (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012857-39 | Sponsor Protocol Number: A4021032 | Start Date*: 2009-11-16 | |||||||||||
Sponsor Name:PFIZER, S.A. | |||||||||||||
Full Title: ESTUDIO DE FASE 2, ALEATORIZADO Y ABIERTO DE FIGITUMUMAB (CP-751,871) MÁS CISPLATINO (O CARBOPLATINO) Y ETOPOSIDO, FRENTE A CISPLATINO (O CARBOPLATINO) Y ETOPOSIDO SOLOS, COMO TRATAMIENTO DE PRIME... | |||||||||||||
Medical condition: Pacientes con cáncer de pulmón microcítico en estadio extendido que no hayan recibido quimioterapia previa para su enfermedad. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) BG (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000906-35 | Sponsor Protocol Number: BAY41-6551/13085 | Start Date*: 2008-11-28 |
Sponsor Name:Bayer Schering Pharma AG | ||
Full Title: A Prospective, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Safety and Efficacy of BAY 41-6551 as Adjunctive Therapy in Intubated and Mechanically-Ventilated Pati... | ||
Medical condition: Gram-negaive pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) HU (Completed) NL (Completed) BE (Completed) ES (Completed) FR (Completed) LV (Prematurely Ended) GR (Completed) PT (Completed) IT (Prematurely Ended) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000149-15 | Sponsor Protocol Number: NEEDS | Start Date*: 2020-04-22 | ||||||||||||||||
Sponsor Name:Karolinska University Hospital | ||||||||||||||||||
Full Title: NEoadjuvant chemoradiotherapy for Esophageal squamous cell carcinoma versus Definitive chemoradiotherapy with salvage Surgery as needed (NEEDS Trial). | ||||||||||||||||||
Medical condition: Resectable locally advanced squamous cell carcinoma (SCC) of the esophagus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) NO (Trial now transitioned) IE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000799-39 | Sponsor Protocol Number: 20-AVP-786-307 | Start Date*: 2021-02-05 | |||||||||||||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||||||||||||
Full Title: A Phase 3, multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy, safety, and tolerability of AVP-786 (deudextromethorphan hydrobromide [d6-DM]/quinidine sulfate [Q... | |||||||||||||||||||||||
Medical condition: Agitation in patients with dementia of the Alzheimer’s type | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Trial now transitioned) SK (Trial now transitioned) NL (Ongoing) SI (Trial now transitioned) HR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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