- Trials with a EudraCT protocol (46)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
46 result(s) found for: RFA.
Displaying page 1 of 3.
EudraCT Number: 2008-000963-41 | Sponsor Protocol Number: 104-06-301 | Start Date*: 2008-12-03 | |||||||||||
Sponsor Name:CELSION CORPORATION | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blinded, Dummy-Controlled Study of the Efficacy and Safety of ThermoDox (Thermally Sensitive Liposomal Doxorubicin) in Combination with Radiofrequency Ablation (R... | |||||||||||||
Medical condition: patients with Non-Resectable Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000934-53 | Sponsor Protocol Number: 104-13-302 | Start Date*: 2014-11-11 | |||||||||||
Sponsor Name:Celsion Corporation | |||||||||||||
Full Title: A Phase III, Randomized, Double Blind, Dummy-Controlled Study of ThermoDox® (Lyso-Thermosensitive Liposomal Doxorubicin-LTLD) in Hepatocellular Carcinoma (HCC) using standardized Radiofrequency Abl... | |||||||||||||
Medical condition: Hepatocellular Carcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004200-38 | Sponsor Protocol Number: N11RFA | Start Date*: 2012-03-28 | ||||||||||||||||
Sponsor Name:NKI-AVL | ||||||||||||||||||
Full Title: Phase II study exploring safety and efficacy of the combination of ipilimumab with radiofrequency ablation (RFA) in patients with unresectable uveal melanoma liver metastasis (SECIRA-UM) | ||||||||||||||||||
Medical condition: Unresectable uveal melanoma liver metastasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012576-27 | Sponsor Protocol Number: SORAMIC | Start Date*: 2010-04-09 | ||||||||||||||||||||||||||
Sponsor Name:Medical Faculty, University Magdeburg | ||||||||||||||||||||||||||||
Full Title: Evaluation of Sorafenib in combination with local micro-therapy guided by Gd-EOB-DTPA enhanced MRI in patients with inoperable hepatocellular carcinoma | ||||||||||||||||||||||||||||
Medical condition: Patients with Hepatocellular carcinoma (liver-predominant disease) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) AT (Completed) ES (Completed) BE (Completed) PL (Completed) SI (Completed) IT (Completed) GB (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001941-11 | Sponsor Protocol Number: 2021-1798 | Start Date*: 2021-09-09 | ||||||||||||||||
Sponsor Name:Rijnstate hospital | ||||||||||||||||||
Full Title: Ultrasound-guided radiofrequency ablation versus radioactive iodine as treatment for hyperthyroidism caused by solitary autonomous thyroid nodules. | ||||||||||||||||||
Medical condition: Patients > 18 years with (subclinical) hyperthyroidism caused by a solitary hyperactive thyroid nodules, either as a solitary hyperactive node in an otherwise normal thyroid gland or as a single hy... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004397-26 | Sponsor Protocol Number: GI1949 | Start Date*: 2020-02-19 | ||||||||||||||||
Sponsor Name:Department of Oncology, Herlev & Gentofte Hospital | ||||||||||||||||||
Full Title: FOLFOX + Immunotherapy with intrahepatic administration of oxaliplatin for patients with multiple non-resectable liver metastasis from colorectal cancer. | ||||||||||||||||||
Medical condition: Liver metastasis from colorectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003774-40 | Sponsor Protocol Number: TheStopGISTtrial | Start Date*: 2016-11-09 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Discontinuation of imatinib in patients with oligo-metastatic gastrointestinal stromal tumor that has become radiologically undetectable with treatment | |||||||||||||
Medical condition: Gastrointestinal stromal tumour (GIST) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000987-11 | Sponsor Protocol Number: 2012/409 | Start Date*: 2012-07-02 | |||||||||||
Sponsor Name:Anni Ravnbek Jensen | |||||||||||||
Full Title: DEBIRI-TACE (DRUG ELUTING BEAD med IRINOTECAN-TRANS ARTERIEL CHEMO EMBOLIZATION) Intrahepatic chemoembolization with irinotecan-containing DC-BEADS combined with systemic chemotherapy and bevac... | |||||||||||||
Medical condition: Metastatic colorectal cancer with metastasis confined to the liver | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003741-42 | Sponsor Protocol Number: 31031981 | Start Date*: 2014-05-06 |
Sponsor Name:Medizinische Universität Innsbruck, Abteilung für Nuklearmedizin | ||
Full Title: PROSPECTIVE STUDY OF [68GA]NODAGA-RGD-PET FOR THE DIAGNOSIS OF HEPATOCELLULAR CARCINOMA AND THE ASSESSMENT OF TREATMENT RESPONSE | ||
Medical condition: This trial investigates a new tracer substance for PET scan of hepatocellular carcinoma in patients with liver disease. The condition investigated is a hepatocellular carcinoma in patients with liv... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002027-42 | Sponsor Protocol Number: POR-ELONVA | Start Date*: 2013-08-14 |
Sponsor Name:INSTITUTO DE INVESTIGACION SANITARIA LA FE | ||
Full Title: PROSPECTIVE AND RANDOMIZED STUDY FOR ASSESSMENT OF CONTROLLED OVARIAN STIMULATION WITH ALFA Corifollitropin IN PATIENTS WITH OVARIAN RESPONSE EXPECTED OR POOR IN VITRO FERTILIZATION CYCLE. | ||
Medical condition: Women who meet the criteria for infertility Bologna | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000566-23 | Sponsor Protocol Number: GK-001-01 | Start Date*: 2008-08-25 | |||||||||||
Sponsor Name:GeneCare Research Institute Co., Ltd. | |||||||||||||
Full Title: A randomized phase 2 double-blind, placebo-controlled study of GK-001 in hepatocellular carcinoma (HCC) in chronic hepatitis C patients after prior curative HCC treatment Estudio aleatorizado de ... | |||||||||||||
Medical condition: hepatocellular carcinoma (HCC) in chronic hepatitis C patients after prior curative HCC treatment carcinoma hepatocelular (CHC) en pacientes con hepatitis C crónica tras tratamiento curativo para... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003288-31 | Sponsor Protocol Number: TUD-CELIM2-050 | Start Date*: 2012-06-04 | ||||||||||||||||
Sponsor Name:Technical University Dresden | ||||||||||||||||||
Full Title: Open, randomized, multicenter phase II trial with cetuximab /5-FU/FA/irinotecan or cetuximab/5-FU/FA /irinotecan/oxaliplatin in ras wild type patients or with irinotecan/oxaliplatin/5-FU/FA with or... | ||||||||||||||||||
Medical condition: The aim of this study is to investigate the following schedules for efficacy with regard to response rate in neoadjuvant treatment of patients with non-resectable liver metastases: - Cetuximab/FOL... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001381-42 | Sponsor Protocol Number: IMMULAB | Start Date*: 2019-01-25 | |||||||||||
Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH am Krankenhaus Nordwest | |||||||||||||
Full Title: IMMULAB – A phase II trial of immunotherapy with pembrolizumab in combination with local ablation for patients with early stage hepatocellular carcinoma (HCC) | |||||||||||||
Medical condition: early stage hepatocellular carcinoma (HCC) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011925-14 | Sponsor Protocol Number: 1199.37 | Start Date*: 2009-08-24 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: A multicenter, open label, phase I / II study to evaluate safety, pharmacokinetics and efficacy of BIBF 1120 in comparison with oral sorafenib for advanced hepatocellular carcinoma patients. | |||||||||||||
Medical condition: Histologically or cytologically confirmed hepatocellular carcinoma not amenable to local therapy with adequate renal, hematological and liver paramenters with Child-Pugh score 7 or less, in 1st lin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) DE (Completed) SK (Completed) HU (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023411-33 | Sponsor Protocol Number: ONC-2009-002 | Start Date*: 2010-11-03 | |||||||||||
Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: A phase II, randomized, double-blind, placebo controlled trial of Sorafenib as adjuvant treatment for hepatocellular carcinoma after TACE-based treatments. | |||||||||||||
Medical condition: hepatocellular carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001375-22 | Sponsor Protocol Number: 1560-GITCG | Start Date*: 2019-04-01 | |||||||||||||||||||||
Sponsor Name:European Organisation for the Research and Treatment of Cancer (EORTC) | |||||||||||||||||||||||
Full Title: EORTC ILOC study: Phase II of immunotherapy plus local tumor ablation (RFA or stereotactic radiotherapy) in patients with colorectal cancer liver metastases | |||||||||||||||||||||||
Medical condition: Metastatic colorectal cancer with Incurable liver metastases | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) SE (Completed) NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003482-18 | Sponsor Protocol Number: RN01-CP-0002 | Start Date*: 2014-03-24 | |||||||||||
Sponsor Name:ReNeuron Ltd | |||||||||||||
Full Title: A Phase II Efficacy Study of Intracerebral CTX0E03 DP In Patients with Stable Paresis of the Arm Following an Ischaemic Stroke. | |||||||||||||
Medical condition: Supratentorial ischaemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002053-38 | Sponsor Protocol Number: MITIGATE-NeoBOMB1 | Start Date*: 2016-11-30 |
Sponsor Name:Medical University Innsbruck | ||
Full Title: A Phase I/IIa study to evaluate safety, biodistribution, dosimetry and preliminary diagnostic performance of 68Ga-NeoBOMB1 in patients with advanced TKI-treated GIST using positron-emission tomogra... | ||
Medical condition: Gastrointestinal stromal tumours previously or currently under TKI-treatment including at least 50% TKI-resistant patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003389-10 | Sponsor Protocol Number: HepaVac-101 | Start Date*: 2017-03-29 | |||||||||||
Sponsor Name:Istituto Nazionale Tumori G. "Pascale" | |||||||||||||
Full Title: A phase I/II trial of IMA970A plus CV8102 following a single pre-vaccination infusion of cyclophosphamide in patients with very early, early and intermediate stage of hepatocellular carcinoma after... | |||||||||||||
Medical condition: Very early, early and intermediate stage hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001590-32 | Sponsor Protocol Number: MMC-2016-01 | Start Date*: 2018-04-19 | |||||||||||
Sponsor Name:Manuel Macía Cortiñas | |||||||||||||
Full Title: Comparison of two protocols of controlled ovarian stimulation with highly purified menotropin in low-responder patients according to Bologna criteria treated in Spanish public hospitals. | |||||||||||||
Medical condition: PRIMARY INFERTILITY | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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