- Trials with a EudraCT protocol (1,285)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,285 result(s) found for: Radiotherapy OR Radiation.
Displaying page 1 of 65.
EudraCT Number: 2006-000329-78 | Sponsor Protocol Number: PMF603-PA1/06 | Start Date*: 2006-06-14 | |||||||||||
Sponsor Name:PROMEFARM | |||||||||||||
Full Title: Naburen enema for prevention of radiation proctitis. A multicentre randomised placebo-controlled dose-finding phase II study to evaluate efficacy, tolerability, acceptability and compliance with en... | |||||||||||||
Medical condition: Radiation Proctitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004236-20 | Sponsor Protocol Number: MN4 | Start Date*: 2008-06-24 |
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE S. MARIA NUOVA | ||
Full Title: PET-CT DIAGNOSIS OF CARCINOMA PROSTATICO WITH ALTERNATIVE TO FLUORODESOSSIGLUCOSIO Radio: 18F-COLINA | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000167-14 | Sponsor Protocol Number: 105-15-201 | Start Date*: 2017-02-16 | |||||||||||
Sponsor Name:CELSION CORPORATION | |||||||||||||
Full Title: HEAT-ACTIVATED TARGET THERAPY RADIOTHERAPY + HYPERTHERMIA + LYSO THERMOSENSITIVE LIPOSOMAL DOXORUBICIN) OF LOCALREGIONAL RELAPSE IN BREAST CANCER PATIENTS | |||||||||||||
Medical condition: Local-Regional Relapse in Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003669-32 | Sponsor Protocol Number: GONO-Sancuso | Start Date*: 2020-07-03 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO DEL NORD OVEST | |||||||||||||
Full Title: GRANISETRON TRANSDERMAL SYSTEM (GTDS) IN PREVENTING NAUSEA AND VOMITING INDUCED BY CISPLATIN-BASED CHEMOTHERAPY AND CONCURRENT RADIOTHERAPY FOR HEAD AND NECK CANCER | |||||||||||||
Medical condition: Head and neck cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002765-36 | Sponsor Protocol Number: IEO38 | Start Date*: 2014-03-23 | |||||||||||
Sponsor Name:Istituto Europeo di Oncologia | |||||||||||||
Full Title: SIB –IMRT using a modulated accelerated fractionation for head and neck cancer patients | |||||||||||||
Medical condition: head and neck squamous cell carcinoma eligible for a curative treatment with radiotherapy and Cetuximab | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002046-20 | Sponsor Protocol Number: IOVHN12012 | Start Date*: 2012-05-28 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO VENETO | |||||||||||||
Full Title: Role of SAMITAL in prevention and treatment of oral mucositis in patients treated with chemo-radiation (CT/RT)for head-and-neck squamous cell carcinomas. A double-blind, Phase 2 placebo controlled,... | |||||||||||||
Medical condition: Head-and-neck cancer (Squamous cell carcinomas) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001938-14 | Sponsor Protocol Number: 60711868 | Start Date*: 2008-03-31 | |||||||||||
Sponsor Name:AVAPO RICERCHE - VENEZIA | |||||||||||||
Full Title: Neoadjuvant docetaxel, cisplatin and 5-fluororacil (TPF) followed by radiotherapy plus concomitant chemotherapy or cetuximab versus radiotherapy plus concomitant chemotherapy or cetuximab in patien... | |||||||||||||
Medical condition: patients with locally advanced squamous cell carcinoma of the head and neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004223-20 | Sponsor Protocol Number: ALRAD | Start Date*: 2012-09-25 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: WEEKLY PEMETREXED (ALIMTA®) AND RADIOTHERAPY IN LOCALLY ADVANCED OR LOCALLY RELAPSED NON-SQUAMOUS NON SMALL CELL LUNG CANCERS (NSCLC) | |||||||||||||
Medical condition: LOCALLY ADVANCED NSCLC CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003765-10 | Sponsor Protocol Number: I-Tackle | Start Date*: 2018-07-10 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Immunotherapy Followed By EGFR Inhibitor In Locally Advanced Or Metastatic Squamous Cell Cancer Of The Skin: Tackling Primary And Secondary Resistance | |||||||||||||
Medical condition: Patient with Locally Advanced Or Metastatic Squamous Cell Cancer Of The Skin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000679-28 | Sponsor Protocol Number: FAZA-gliomi | Start Date*: 2015-07-13 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: Prognostic value of 18F-FAZA PET/CT in high grade glioma: comparison with MRI and correlation with hypoxia biomarkers. | |||||||||||||
Medical condition: Patients with high-grade glioma (III-IV). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001385-38 | Sponsor Protocol Number: WIN-HYPO2021 | Start Date*: 2021-08-18 | |||||||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||||||||||||
Full Title: RANDOMIZED STUDY TO PROTECT FROM RADIATION IATROGENIC HYPOTHYROIDISM PATIENTS WITH MEDULLOBLASTOMA (ANY AGE, STAGE AND ANY BIOLOGICAL RISK) AND PEDIATRIC PATIENTS WITH HODGKIN LYMPHOMA AND NON-HODG... | |||||||||||||||||||||||
Medical condition: medulloblastoma, Hodgkin and non-Hodgkin lymphomas | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019216-20 | Sponsor Protocol Number: AZ2010 | Start Date*: 2010-05-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | |||||||||||||
Full Title: "Effects of drug treatment with bisphosphonates (zoledronic acid) in the prevention of skeletal events in breast cancer patients with osteoporosis. Significant correlation with some biological para... | |||||||||||||
Medical condition: Breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001271-20 | Sponsor Protocol Number: MOLT-2013-02 | Start Date*: 2013-08-12 | |||||||||||
Sponsor Name:L. Molteni & C dei F.lli Alitti Società di Esercizio S.p.A. | |||||||||||||
Full Title: A multicenter randomized open trial to evaluate the efficacy of fentanyl pectin nasal spray (FPNS) versus Physician Choice (PC) - Usual Care (UC), in reducing incidental predictable breakthrough pa... | |||||||||||||
Medical condition: Patients with head and neck cancer undergoing radiotherapy with uncontrolled pain at swallowing (moderate/severe intensity). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005638-20 | Sponsor Protocol Number: CRO-2010-14 | Start Date*: 2011-02-18 | |||||||||||
Sponsor Name:CENTRO DI RIFERIMENTO ONCOLOGICO DI AVIANO | |||||||||||||
Full Title: Phase III randomized trial of preoperative radiotherapy with an integrated simultaneous boost IMRT-IGRT) versus chemoradiotherapy for T3-4 rectal cancer | |||||||||||||
Medical condition: Patients with operable rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003680-25 | Sponsor Protocol Number: CNAO_44-2021C_ICONIC | Start Date*: 2021-12-14 | ||||||||||||||||
Sponsor Name:Fondazione CNAO Centro Nazionale di Adroterapia Oncologica | ||||||||||||||||||
Full Title: Immune checkpoint inhibitors and Carbon iON radiotherapy In solid Cancers with stable disease (ICONIC) | ||||||||||||||||||
Medical condition: • Unresectable or metastatic melanoma • Locally advanced or metastatic non-small cell lung cancer (NSCLC) • Untreated recurrent/metastatic head & neck sqamous cell carcinoma (HNSC... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003652-21 | Sponsor Protocol Number: 2019-23 | Start Date*: 2020-01-23 | |||||||||||
Sponsor Name:OSPEDALE CLASSIFICATO EQUIPARATO SACRO CUORE DON CALABRIA - PRESIDIO OSPEDALIERO ACCREDITATO | |||||||||||||
Full Title: Interventional two arms open-label study for evaluating the diagnostic performance of PET PSMA in patients affected by biochemical recurrent prostate cancer. | |||||||||||||
Medical condition: Biochemical recurrent prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003127-41 | Sponsor Protocol Number: BT009E | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:INSIGHTEC | |||||||||||||
Full Title: Assessment of Safety and Feasibility of Exablate Blood-Brain Barrier Disruption (BBBD) with Microbubble Resonators for the Treatment of Recurrent Glioblastoma (rGBM) in Subjects Undergoing Carbopla... | |||||||||||||
Medical condition: Recurrent Glioblastoma (rGBM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007152-94 | Sponsor Protocol Number: 02-2008 | Start Date*: 2009-01-30 | |||||||||||
Sponsor Name:I.T.M.O. - ITALIAN TRIALS IN MEDICAL ONCOLOGY | |||||||||||||
Full Title: Efficacy and Safety of RAD001 (Everolimus) in Patients Affected by Biliary Tract Cancer Progressing After Prior Chemotherapy: a Phase II I.T.M.O. Study | |||||||||||||
Medical condition: Patients affected by biliary tract cancer progressing after prior chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005877-31 | Sponsor Protocol Number: ZK219477-01 | Start Date*: 2006-03-27 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: Phase II study Systemic treatment with ZK219477 EPOTHILONE in recurrent Glioblastoma patients | |||||||||||||
Medical condition: Recurrent Glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001252-22 | Sponsor Protocol Number: MP-LALC | Start Date*: 2017-08-02 | |||||||||||
Sponsor Name:DIPARTIMENTO DI ONCOLOGIA-UNIVERSITA' DEGLI STUDI DI TORINO | |||||||||||||
Full Title: Pembrolizumab (MK-3475) as maintainance unresectable stage III NSCLC after chemo-radiotherapy (MP-LALC- Maintainance Pembrolizumab in Locally Advanced Lung Cancer). | |||||||||||||
Medical condition: unresectable stage IIIA/B Non Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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