- Trials with a EudraCT protocol (2,345)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
2,345 result(s) found for: Liver tumor.
Displaying page 1 of 118.
EudraCT Number: 2007-003275-40 | Sponsor Protocol Number: 63/2007/O/Sper | Start Date*: 2008-07-29 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: New immunosuppressive treatments to reduce the rate of recurrence of hepatocellular carcinoma after liver transplantation | |||||||||||||
Medical condition: Liver transplantation in patients with hepatocellular carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001503-19 | Sponsor Protocol Number: IEO S 238/205 | Start Date*: 2005-07-06 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: CLINICAL AND BIOLOGICAL STUDY ON THE ADMINISTRATION OF THALIDOMIDE IN PATIENTS WITH PRIMARY CANCER OF THE LIVER | |||||||||||||
Medical condition: PRIMARY CANCER OF THE LIVER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000747-10 | Sponsor Protocol Number: 2154/2006 | Start Date*: 2006-07-21 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: PHASE II STUDY OF BAY 43-9006 AND INFUSIONAL 5-FLUOROURACIL IN ADVANCED HEPATOCELLULAR CARCINOMA | |||||||||||||
Medical condition: patients with advanced inoperable hepatocellular carcinoma Child A or B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003034-15 | Sponsor Protocol Number: 60/2006/O/Sper | Start Date*: 2006-07-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Trattamento dell’epatocarcinoma (HCC) mediante chemioembolizzazione (TACE) selettiva tradizionale versus TACE selettiva con microsfere caricate con Doxorubicina: studio monocentrico, randomizzato, ... | |||||||||||||
Medical condition: Hepatocarcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-006053-25 | Sponsor Protocol Number: IOM/BRA/034 | Start Date*: 2006-08-02 | |||||||||||
Sponsor Name:Bracco ALTANA Pharma GmbH | |||||||||||||
Full Title: PET/CT WITH IOMERON® 400 IN PATIENTS WITH SUSPECTED MALIGNANT LIVER LESIONS - A FEASIBILITY STUDY | |||||||||||||
Medical condition: Indication for POSITRON EMISSION TOMOGRAPHY (PET MeDRA 9.0 LLT 10036223) and Computed tomography (Computerized tomography (CT MeDRA 9.0 LLT 10062404) in patients with highly suspected or proved m... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022730-91 | Sponsor Protocol Number: BR1-130 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:Bracco Imaging S.p.A. | |||||||||||||
Full Title: Characterization of focal liver lesions with Sonovue(R)-enhanced ultrasound imaging: a phase III, intrapatient comparative study versus unenhanced ultrasound imaging using histology or combined ... | |||||||||||||
Medical condition: At least one focal liver lesion requiring further work-up for complete characterization. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004649-18 | Sponsor Protocol Number: 13001 | Start Date*: 2014-02-21 | |||||||||||
Sponsor Name:Jens Hilligsø | |||||||||||||
Full Title: The effect of phrenic nerve block on postoperative shoulder pain in patients for liver resection – a double blinded randomised controlled trial. | |||||||||||||
Medical condition: Posteoperative shoulder pain following open liver resection surgery . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013870-42 | Sponsor Protocol Number: BOOST | Start Date*: 2011-10-11 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: Sorafenib in the first line treatment of advanced hepatocellular carcinoma with ChildPugh liver function class B. Multicentre phase 3 randomized trial | |||||||||||||
Medical condition: advanced hepatocellular carcinoma with ChildPugh liver function class B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003028-22 | Sponsor Protocol Number: RGT100-001 | Start Date*: 2017-01-26 | |||||||||||||||||||||
Sponsor Name:Rigontec GmbH | |||||||||||||||||||||||
Full Title: A Phase I/II, Multicenter, Open-label, Clinical Trial of Intratumoral/Intralesional Administration of RGT100 in Subjects with Advanced or Recurrent Tumors | |||||||||||||||||||||||
Medical condition: Advanced or recurrent tumors | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Prematurely Ended) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-003423-23 | Sponsor Protocol Number: P070134 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Etude de phase II nationale multicentrique évaluant l’activité antitumorale du sunitinib (SUTENT) chez des patients atteints d’hépatocarcinomes fibrolamellaires inopérables d’emblée ou en rechute n... | |||||||||||||
Medical condition: patients atteints d'hépatocarcinome fibrolamellaire non opérable ou en échec du traitement chiruirgical | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005183-82 | Sponsor Protocol Number: 12/2005/O/Sper | Start Date*: 2005-09-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Intra-Arterial hepatic administration of SIR-Spheres for the advanced HEPATOCARCINOMA. CLINICAL TRIAL OF PHASE II | |||||||||||||
Medical condition: Hepatocarcinoma HCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000758-30 | Sponsor Protocol Number: ONC-2006-004 | Start Date*: 2007-03-07 | |||||||||||
Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Randomized continuation, dose escalation trial of Sorafenib in pts with advanced HCC with radiological progression on prior sorafenib treatment (Phase II study) | |||||||||||||
Medical condition: Hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000834-21 | Sponsor Protocol Number: POCHER-2/AIRC11770 | Start Date*: 2012-04-01 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: Molecular Biomarkers for Colorectal Liver Metastases Resectability after Chemotherapy with Cetuximab | |||||||||||||
Medical condition: PATIENTS WITH LIVER COLORECTAL METASTASES NOT CANDIDATED TO SURGERY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005197-51 | Sponsor Protocol Number: 14650 | Start Date*: 2008-07-24 | |||||||||||
Sponsor Name:The Netherlands Cancer Institute/ Antoni van Leeuwenhoek hospital [...] | |||||||||||||
Full Title: Accelerated growth of synchronous colorectal liver metastases: effects of neo-adjuvant therapy | |||||||||||||
Medical condition: synchronous liver metastases in patients with the primary colorectal tumour in situ | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000270-28 | Sponsor Protocol Number: NL75171.058.20 | Start Date*: 2022-06-30 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Selective Indocyanine Green Injection of a Segmental Hepatic Artery Followed by Near-Infrared Fluorescence Guided Anatomical Liver Resection: A Feasibility Study | ||
Medical condition: Hepatocellular carcinoma, hepatic adenoma, intrahepatic cholangiocarcinoma, colorectal liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005284-98 | Sponsor Protocol Number: CATROP-2007 | Start Date*: 2009-02-20 | |||||||||||||||||||||
Sponsor Name:Servicio de Anestesiología y Reanimación | |||||||||||||||||||||||
Full Title: Ensayo Clínico aleatorio y a doble cieo de eficacia analgésica postoperatoria en cirugía colo-rectal y cirugía hepática con infusión contínua de anestesico local verus suero salino en la incisión q... | |||||||||||||||||||||||
Medical condition: Dolor postoperatorio en pacientes sometidos a tratamiento quirúrgico de neoplasia colo-rectal o bien a cirugía hepática | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002930-62 | Sponsor Protocol Number: GDX-44-008 | Start Date*: 2016-11-17 | |||||||||||
Sponsor Name:GUERBET | |||||||||||||
Full Title: Proof of Concept study concerning efficacy of P03277 MR Imaging in HCC diagnosis Phase IIa Clinical Study | |||||||||||||
Medical condition: liver nodules of less or equal to 3 cm suspected for HCC in subjects with chronic liver disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006097-76 | Sponsor Protocol Number: LOTUS | Start Date*: 2013-01-11 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: RANDOMIZED PHASE 3 TRIAL EVALUATING THE EFFICACY OF LOCOREGIONAL TREATMENT WITH TRANSARTERIAL EMBOLIZATION (TAE) FOR LIVER METASTASIS, IN COMBINATION WITH OCTREOTIDE LAR, IN PATIENTS WITH NEUROENDO... | |||||||||||||
Medical condition: PATIENTS WITH NEUROENDOCRINE TUMOR AND INOPERABLE LIVER METASTASIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000369-54 | Sponsor Protocol Number: 60725 | Start Date*: 2018-06-27 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Intra-arterial Lutetium-177- dotatate for treatment of patients with neuroendocrine tumor liver metastases | ||
Medical condition: Patients with neuro-endocrine tumors with liver metastases with an indication for treatment with lutetium-177-dotatate | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000525-30 | Sponsor Protocol Number: A6181055 | Start Date*: 2006-06-14 | |||||||||||
Sponsor Name:Pfizer Hellas A.E. | |||||||||||||
Full Title: AN OPEN LABEL INTERNATIONAL MULTI-CENTER PHASE 2 ACTIVITY AND SAFETY STUDY OF SU011248 IN PATIENTS WITH UNRESECTABLE HEPATOCELLULAR CARCINOMA | |||||||||||||
Medical condition: Histologically confirmed diagnosis of hepatocellular carcinoma. Patients with the fibrolamellar histology or a mixed histology are not eligible. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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