- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
17 result(s) found for: Renal fascia.
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EudraCT Number: 2008-005782-59 | Sponsor Protocol Number: 08/0136 | Start Date*: 2010-09-29 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: ARISTOTLE - A phase III trial comparing standard versus novel CRT as pre-operative treatment for MRI defined locally advanced rectal cancer. | ||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||
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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: 2020-004167-29 | Sponsor Protocol Number: NA | Start Date*: 2021-03-15 |
Sponsor Name:CHU de Liège | ||
Full Title: Study of the noninferiority of an oral versus intravenous administration of tranexamic acid in total hip arthroplasty | ||
Medical condition: Bleeding in total hip arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002333-29 | Sponsor Protocol Number: GEMCAD-1601 | Start Date*: 2017-04-19 | |||||||||||
Sponsor Name:GEMCAD (Grupo Español Multidisciplinar en Cáncer Digestivo) | |||||||||||||
Full Title: Preoperative induction therapy with 12 weeks of Panitumumab in combination with mFOLFOX-6 in an enriched population (Quadruple Wild-Type) of patients with mrT3 rectal cancer of the middle third wit... | |||||||||||||
Medical condition: Patients with rectal adenocarcinoma of intermediate risk (defined by magnetic resonance imaging [MRI]), without mutations in KRAS, BRAF, NRAS and PI3KCA, who are candidates for preoperative treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007177-23 | Sponsor Protocol Number: Mo19051 | Start Date*: 2008-11-12 | ||||||||||||||||
Sponsor Name:U.Z. Gasthuisberg | ||||||||||||||||||
Full Title: A randomized phase II of bevacizumab, capecitabine and radiation therapy with or without oxaliplatin in the preoperative treatment of locally advanced rectal cancer | ||||||||||||||||||
Medical condition: locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024354-11 | Sponsor Protocol Number: ABCSGR05 | Start Date*: 2011-03-03 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: Preoperative induction chemotherapy in combination with Bevacizumab followed by combined chemoradiotherapy in locally advanced rectal cancer with high risk of recurrence- phase II pilot study with ... | ||
Medical condition: locally advanced rectal cancer with high risk of recurrence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002310-22 | Sponsor Protocol Number: 35/2008/O/Sper | Start Date*: 2008-06-16 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | ||||||||||||||||||
Full Title: A multicenter phase II trial of Recipient pre-treatment with Short-Term Rapamycin for the prevention of acute GVHD after hematopoietic stem cell transplantation in Elderly Patients | ||||||||||||||||||
Medical condition: Graft Versus Host Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023083-40 | Sponsor Protocol Number: SPON830-10 | Start Date*: 2012-03-19 |
Sponsor Name:Cardiff University | ||
Full Title: A Phase II study of neoadjuvant chemotherapy given before SCPRT as treatment for patients with MRI-staged operable rectal cancer at high risk of metastatic relapse | ||
Medical condition: Rectal adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-002063-14 | Sponsor Protocol Number: GEMCAD-1402 | Start Date*: 2014-10-23 | |||||||||||
Sponsor Name:GEMCAD (Grupo Español Multidisciplinar en Cáncer Digestivo) | |||||||||||||
Full Title: Induction FOLFOX with or without Aflibercept followed by chemoradiation in High Risk Locally Advanced Rectal Cancer. Phase II randomized, multicenter, open label trial | |||||||||||||
Medical condition: Patients with high risk locally advanced rectal carcinoma (defined by Magnetic Resonance Imaging [MRI]), who are candidates for multimodality treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023957-12 | Sponsor Protocol Number: RAPIDO | Start Date*: 2011-03-29 | |||||||||||
Sponsor Name:Dutch Colorectal Cancer Group [...] | |||||||||||||
Full Title: Randomized Multicentre Phase III study of short course radiation therapy followed by prolonged pre-operative chemotherapy and surgery in primary high risk rectal cancer compared to standard chemor... | |||||||||||||
Medical condition: primary rectal cancer without detectable distant metastasis, but with a high risk to relapse locally or systemically. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) NL (Ongoing) ES (Ongoing) SI (Ongoing) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003340-45 | Sponsor Protocol Number: TRUST | Start Date*: 2012-02-23 | |||||||||||
Sponsor Name:ARCO | |||||||||||||
Full Title: OPEN-LABEL PHASE II STUDY OF INDUCTION TREATMENT WITH FOLFOXIRI PLUS BEVACIZUMAB FOLLOWED BY PREOPERATIVE CHEMORADIOTHERAPY PLUS BEVACIZUMAB IN PATIENTS WITH LOCALLY ADVANCED, RESECTABLE RECTAL CANCER | |||||||||||||
Medical condition: Advanced Rectal Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000763-33 | Sponsor Protocol Number: 20160283 | Start Date*: 2017-12-01 |
Sponsor Name:Amgen, Inc. | ||
Full Title: A Phase 1b/2 Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of Efavaleukin Alfa in Adult Subjects with Steroid Refractory Chronic Graft versu... | ||
Medical condition: Steroid Refractory Chronic Graft versus Host Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001356-35 | Sponsor Protocol Number: ACO/ARO/AIO-18.2 | Start Date*: 2020-08-04 | |||||||||||
Sponsor Name:University of Heidelberg | |||||||||||||
Full Title: ACO/ARO/AIO-18.2 Preoperative FOLFOX versus postoperative risk-adapted chemotherapy in patients with locally advanced rectal cancer and low risk for local failure: A randomized phase III trial of ... | |||||||||||||
Medical condition: Locally advanced rectal adenocarcinoma localized 0 - 16 cm from the anal verge with low risk of local failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001471-36 | Sponsor Protocol Number: PrimeRT-2018 | Start Date*: 2020-10-05 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Priming the Tumour MicroEnvironment for Effective Treatment with Immunotherapy in Locally Advanced Rectal Cancer: A Phase II trial of Durvulamab in Combination with Extended Neoadjuvant Regimens i... | |||||||||||||
Medical condition: Rectal Cancer. | |||||||||||||
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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: 2015-002773-38 | Sponsor Protocol Number: AIO-KRK-0214 | Start Date*: 2016-12-20 | |||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||
Full Title: mFOLFOX6 vs. mFOLFOX6 + aflibercept as neoadjuvant treatment in MRI-defined T3-rectal cancer: a randomized phase-II-trial | |||||||||||||||||||||||
Medical condition: Patients with locally advanced rectal or rectosigmoid cancer staged cT3 CRM-negative with MRI | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023484-17 | Sponsor Protocol Number: 2010-023484-17 | Start Date*: 2011-06-11 | |||||||||||
Sponsor Name:ITALIAN SARCOMA GROUP | |||||||||||||
Full Title: LOCALIZED HIGH-RISK SOFT TISSUE SARCOMAS OF THE EXTREMITIES AND TRUNK WALL IN ADULTS: AN INTEGRATING APPROACH COMPRISING STANDARD VS HISTOTYPE-TAILORED NEOADJUVANT CHEMOTHERAPY (ISG-STS 10-01) | |||||||||||||
Medical condition: High risk localized soft tissue sarcomas typical of the adult | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Ongoing) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001599-18 | Sponsor Protocol Number: BAY 12-8039/11974 | Start Date*: 2006-11-03 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A prospective, randomized, double dummy, double blind, multinational, multicenter trial comparing the safety and efficacy of sequential (intravenous/oral) moxifloxacin 400 mg once daily to intraven... | |||||||||||||
Medical condition: complicated skin and skin structure Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) BE (Completed) LV (Completed) FR (Completed) GR (Completed) IE (Completed) HU (Completed) ES (Completed) NL (Prematurely Ended) AT (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001128-11 | Sponsor Protocol Number: BO20289 | Start Date*: 2007-12-14 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd, Pharmaceuticals Divison, PDR | |||||||||||||
Full Title: An international multi-centre open-label 2-arm phase III trial of adjuvant bevacizumab in triple negative breast cancer. | |||||||||||||
Medical condition: Early primary invasive adenocarcinoma of the breast (triple negative and/or basel-like phenotype) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) AT (Completed) NL (Completed) BE (Completed) CZ (Completed) GR (Completed) FI (Completed) DE (Completed) IT (Completed) ES (Completed) PT (Completed) SE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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