- Trials with a EudraCT protocol (265)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
265 result(s) found for: Carcinogenesis.
Displaying page 1 of 14.
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: 2005-004614-32 | Sponsor Protocol Number: IEO S262/505 | Start Date*: 2006-01-20 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Randomized phase II trial of Budesonide Turbuhaler 800 micrograms/twice daily versus placebo in high-risk population with undetermined lung nodules detected at screening low dose CT scan | |||||||||||||
Medical condition: Intermediate biomarker modulation in lung carcinogenesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010921-38 | Sponsor Protocol Number: MDL_2009_27155 | Start Date*: 2009-09-08 | |||||||||||
Sponsor Name:UMC Utrecht | |||||||||||||
Full Title: Chemopreventive effects of 5-ASA and UDCA in Ulcerative Colitis: A Double-blind, Randomized Placebo-controlled Pilot Study | |||||||||||||
Medical condition: Ulcerative Colitis and the risk of developing colorectal cancer. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003820-37 | Sponsor Protocol Number: IGIT-008 | Start Date*: 2005-02-10 | |||||||||||
Sponsor Name:Bracco Imaging Spa | |||||||||||||
Full Title: A multicentre study to evaluate the Contibution of SonoVue® and CnTI technology (Contrast Tuned Imaging) to a correct classification of Adnexal Masses as benign or malignant | |||||||||||||
Medical condition: COMPLEX ADNEXAL MASS IN PELVIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000386-31 | Sponsor Protocol Number: OPTO-01-2015(pROSAM) | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
Full Title: Role of SAMITAL in pediatric age ¿ a feasibility study in children with/or at risk of oral mucositis due to chemotherapy and/or radiotherapy | |||||||||||||
Medical condition: Children affected or at risk of oral mucositis from chemoterapy and/or radiotherapy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003676-38 | Sponsor Protocol Number: INT-OM2-001 | Start Date*: 2005-09-13 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: CAPECITABINE TIME TABLE AND RADIOTHERAPY AS ADJUVANT THERAPY IN RECTAL CANCER | |||||||||||||
Medical condition: This trial evaluates safety diarrhea, proctitis and cistitis of Grade 3/4 of radiochemotherapy with time table Capecitabine as adjuvant treatment in rectal cancer after radical surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020678-41 | Sponsor Protocol Number: FARM7SJ7X9 | Start Date*: 2009-07-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: USE OF SORAFENIB IN THE PREVENTION OF RELAPSE OF RESECTED/ABLATED HEPATOCELLULAR CARCINOMA (HCC) IN PATIENTS WITH HEPATITIS C VIRUS CHRONIC INFECTION. | |||||||||||||
Medical condition: Patients HCV RNA positive with HCC, surgical resection or percutaneous tumor ablation procedures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001325-28 | Sponsor Protocol Number: GOIM21003 | Start Date*: 2012-07-17 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: non-Pegylated liposomal doxrubicina (Myocet) + cyclophosphamide versus non pegylated liposomal doxorubicin (Myocet) + metronomic cyclophosphamide in metastatic breast cancer-a multicenter randomize... | |||||||||||||
Medical condition: patients wiyh metastatic breast cancer her2 negative first line treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000393-35 | Sponsor Protocol Number: GOIM21002 | Start Date*: 2012-02-01 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: a multicenter phase II trial of nab-paclitaxel and capecitabine as first line treatment in Her-2 negative metastatic breast cancer (MBC) | |||||||||||||
Medical condition: metastatic breast cancer (MBC) Her-2 negative as first line treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006176-39 | Sponsor Protocol Number: GOIM21001 | Start Date*: 2012-07-12 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: Paclitaxel + Bevacizumab versus doxorubicina liposomiale non pegilata (Myocet), cyclophosfamide e Bevacizumab as the first line treatment in HER-2 negative metastatic breast cancer. Multicenter ran... | |||||||||||||
Medical condition: metastatic breast cancer HER2 negative | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000466-33 | Sponsor Protocol Number: PT/11/2015 | Start Date*: 2016-03-22 | |||||||||||
Sponsor Name:Department of Pediatric oncology, Aarhus University hospital | |||||||||||||
Full Title: Pharmacokinetics and pharmacodynamics of Piperacillin-Tazobactam (PT) in pediatric oncology patients with fever and neutropenia. | |||||||||||||
Medical condition: Pediatric oncology patients with fever and neutropenia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000409-67 | Sponsor Protocol Number: A933/03 | Start Date*: 2005-09-12 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: NON FORNITO | |||||||||||||
Medical condition: THERAPY OF PAIN IN PATIENTS WITH NEOPLASMS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003002-10 | Sponsor Protocol Number: GINECO-EN101 | Start Date*: 2007-10-09 | |||||||||||
Sponsor Name:ARCAGY-GINECO | |||||||||||||
Full Title: A multicentre phase II study, estimating the efficiency and the tolerance of RAD001 (Everolimus) , in patients with endometrial metastatic cancer resistant to a first line of chemotherapy | |||||||||||||
Medical condition: Endometrial metastatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003742-42 | Sponsor Protocol Number: IOR 100 05 | Start Date*: 2006-08-17 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO ROMAGNOLO | |||||||||||||
Full Title: A dose finding phase II study of Alimta in i.v. continuous infusion in patients with malignant pleural mesothelioma, non small cell lung cancer, pancreatic cancer and breast cancer | |||||||||||||
Medical condition: malignant pleural mesothelioma, non small cell lung cancer, pancreatic cancer and breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000513-36 | Sponsor Protocol Number: VIRN2012 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:A.U.S.L. RIMINI | |||||||||||||
Full Title: Validation of the use of lymphography with green indocyanine in identifying the sentinel node in breast cancer | |||||||||||||
Medical condition: WOMAN BREAST CANCER | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017094-38 | Sponsor Protocol Number: GOIRC03/2009 | Start Date*: 2010-03-15 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA | |||||||||||||
Full Title: Gene expression as predictive markers of outcome in non-small cell lung cancer patients (stage IIIB with pleural effusion and stage IV) treated with chemotherapy. Phase II trial of GOIRC. | |||||||||||||
Medical condition: patients with non-small cell lung cancer cells in stage IIIB (with supraclavicular lymphnode metastases and / or pleural effusion) or IV, not previously treated with chemotherapy for advanced disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002784-10 | Sponsor Protocol Number: CESM | Start Date*: 2012-07-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE S. MARIA NUOVA | |||||||||||||
Full Title: Clinical trial comparing contrast enhanced spectral digital mammography (CESM) and magnetic resonance imaging (MRI) to evaluate the effectiveness of neoadjuvant chemotherapy in patients with locall... | |||||||||||||
Medical condition: patient with cito-istologic diagnosis of locally advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024298-37 | Sponsor Protocol Number: ESOT/1/2010 | Start Date*: 2011-03-28 | |||||||||||
Sponsor Name:Dipartimento Integrato di Oncologia, Ematologia e Patologie dell'Apparato Respiratorio | |||||||||||||
Full Title: Early strong opiod treatment in cancer pain -Morphine vs weak opiods | |||||||||||||
Medical condition: Tumor Pain, mild-moderate intensity (VAS 3-7) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006449-14 | Sponsor Protocol Number: CHUBX2008/31 | Start Date*: 2009-02-13 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Evaluation méthodologique de la tomographie par émission de positons couplée au scanner (TEP-TDM) au Fluoromisonidazole marqué au fluor 18 ([18F]-FMISO) dans l’évaluation de la réponse au traitemen... | |||||||||||||
Medical condition: Glioblastome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004126-17 | Sponsor Protocol Number: GOIM22001 | Start Date*: 2013-03-04 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: Cisplatin and capecitabine (ECX) in stomach adenocarcinoma()tratment in advanced stage.Multicenter randomized phase II trial foolwed by GOIM. | |||||||||||||
Medical condition: Gastric Cancer HER2 negative | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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