- Trials with a EudraCT protocol (3,945)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,945 result(s) found for: Liver Diseases.
Displaying page 2 of 198.
| EudraCT Number: 2013-004644-28 | Sponsor Protocol Number: 13-129 | Start Date*: Information not available in EudraCT |
| Sponsor Name:RWTH Aachen University, represented by the Rector, himself, represented by the Dean of the Medical Faculty | ||
| Full Title: Administration of Rifaximin to improve Liver Regeneration and Outcome following Major Liver Resection | ||
| Medical condition: Patients undergoing major liver resection will be included into the study | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-002079-16 | Sponsor Protocol Number: E2013_PK_CASPO70_LIVERFAILURE | Start Date*: 2013-09-05 | |||||||||||
| Sponsor Name:Hospital Erasme | |||||||||||||
| Full Title: Pharmacokinetics of Caspofungin after one dose in patients with liver failure. | |||||||||||||
| Medical condition: The pharmacokinetics parameters of caspofungin will be studied for the patient admitted for alcoholic hepatitis or decompensated cirrhosis (Child-Pugh score 7-15). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001581-20 | Sponsor Protocol Number: IRRB/72/14 | Start Date*: 2018-02-08 | |||||||||||||||||||||
| Sponsor Name:ISTITUTO MEDITERRANEO PER I TRAPIANTI E TERAPIE AD ALTA SPECIALIZZAZIONE - ISMETT | |||||||||||||||||||||||
| Full Title: THE ADDITION OF SIMVASTATIN ADMINISTRATION TO COLD STORAGE SOLUTION OF EXPLANTED WHOLE LIVER GRAFTS FOR FACING ISCHEMIA/REPERFUSION INJURY IN AN AREA WITH LOW RATE OF DECEASED DONATION. A MONOCENT... | |||||||||||||||||||||||
| Medical condition: ISCHEMIC REPERFUSION INJURY AFTER LIVER TRANSPLANTATION: HEPATIC ISCHEMIA AND REPERFUSION INJURY REPRESENTS THE MAIN UNDERLYING MECHANISM FOR GRAFT DYSFUNCTION, AND FAILURE, POST-TRANSPLANTATION. H... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||||||||||||
| 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: 2012-002105-22 | Sponsor Protocol Number: EVL-VHC-HVH.12 | Start Date*: 2012-08-17 | ||||||||||||||||
| Sponsor Name:Dra Itxarone Bilbao. Servicio de cirugía hepatobiliopancreatica y trasplantes. HUVH | ||||||||||||||||||
| Full Title: Personal monitoring of liver transplant patients infected with Hepatitis C Virus. Pilot study to compare the evolution of Hepatitis C by receiving immunosuppression with tacrolimus in combination w... | ||||||||||||||||||
| Medical condition: Recurrence of hepatitis C post-liver transplantation in patients with hepatitic C. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-004031-23 | Sponsor Protocol Number: E2012AILIVER | Start Date*: 2014-08-26 | |||||||||||
| Sponsor Name:Hopital Erasme | |||||||||||||
| Full Title: Serum pharmacokinetics of Caspofungin in patients with liver failure. | |||||||||||||
| Medical condition: The patient admitted for alcoholic hepatitis or decompensated cirrhosis (Child-Pugh score of 10-15) presenting with invasive aspergillosis (proven or probable) and treated by caspofungin. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002214-17 | Sponsor Protocol Number: NL78220.029.21 | Start Date*: 2023-04-24 | ||||||||||||||||
| Sponsor Name:Amsterdam University Medical Centers | ||||||||||||||||||
| Full Title: COLLISION RELAPSE trial - Recurrent colorectal liver metastases: repeat local treatment +/- neoadjuvantsystemic therapy - a phase III prospective randomized controlled trial | ||||||||||||||||||
| Medical condition: Recurrent colorectal liver metastases | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-004325-91 | Sponsor Protocol Number: CRAD001HIT34 | Start Date*: 2014-01-25 | |||||||||||
| Sponsor Name:NOVARTIS FARMA S.p.A | |||||||||||||
| Full Title: Multicenter, prospective, open-label, controlled, randomized, parallel groups study to evaluate the renal function of adult liver transplant recipients treated with two everolimus-based immunosuppr... | |||||||||||||
| Medical condition: liver transplant | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002510-13 | Sponsor Protocol Number: TROMBOFIBtrial | Start Date*: 2018-09-28 | |||||||||||
| Sponsor Name:Antoni Sabaté Pes (Servicio de Anestesiología y Reanimación) del Hospital Universitari de Bellvitge | |||||||||||||
| Full Title: Impact of two thrombelastography-guided strategies of fibrinogen correction on blood product requirements in liver transplantation: a multicenter, randomized trial. TROMBOFIB trial | |||||||||||||
| Medical condition: Liver transplantation is a special risk situation for acute and severe bleeding determined by the complexity of the surgical procedure and by the alteration of haemostasis and coagulation factors, ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000252-34 | Sponsor Protocol Number: CA2099DW | Start Date*: 2020-02-17 | ||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
| Full Title: A Randomized, Multi-center, Phase 3 Study of Nivolumab in Combination with Ipilimumab Compared to Sorafenib or Lenvatinib as First-Line Treatment in Participants with Advanced Hepatocellular Carcinoma | ||||||||||||||||||
| Medical condition: Hepatocellular Carcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) GB (GB - no longer in EU/EEA) ES (Ongoing) PL (Trial now transitioned) BE (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-000232-34 | Sponsor Protocol Number: NASIR-HCC | Start Date*: 2017-09-11 | |||||||||||
| Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
| Full Title: A multicenter, open-label, single-arm study of the safety and antitumoral efficacy of nivolumab in combination with selective internal radiation therapy (SIRT) using SIR-Spheres for the treatment o... | |||||||||||||
| Medical condition: Hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2011-005909-79 | Sponsor Protocol Number: PRIGA | Start Date*: 2012-04-12 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Magnetic resonance with gadoxetic acid for the diagnosis of hepatocellular carcinoma in patients with liver cirrhosis. Evaluation of its impact for the non-invasive diagnosis. | |||||||||||||
| Medical condition: hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-001617-34 | Sponsor Protocol Number: FG-506-01-27 | Start Date*: 2005-03-07 | |||||||||||
| Sponsor Name:Astellas Pharma GmbH | |||||||||||||
| Full Title: AN OPEN, RANDOMISED, MULTICENTRE, CLINICAL STUDY TO COMPARE THE SAFETY AND EFFICACY OF TACROLIMUS AND MINIMAL STEROIDS IN COMBINATION WITH EITHER A MONOCLONAL ANTI-IL2R ANTIBODY (DACLIZUMAB) OR MYC... | |||||||||||||
| Medical condition: Patients with hepatic disease who will undergo primary orthotopic liver or split liver allograft transplantation. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) SE (Completed) FI (Completed) DK (Completed) ES (Completed) IT (Completed) BE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003528-29 | Sponsor Protocol Number: CCHI621ADE04 | Start Date*: 2016-04-14 | ||||||||||||||||
| Sponsor Name:Novartis Pharma GmbH | ||||||||||||||||||
| Full Title: A Multicenter, Open-label, Randomized, Two Arm Study to Investigate the Efficacy and Safety of a Therapy Avoiding Intraoperative Steroids in Combination With Basiliximab, Cyclosporine/Cyclosporine ... | ||||||||||||||||||
| Medical condition: Liver Transplantation Infection | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-005650-54 | Sponsor Protocol Number: MD2011.01 | Start Date*: 2012-06-04 | ||||||||||||||||||||||||||
| Sponsor Name:University Medical Center Groningen | ||||||||||||||||||||||||||||
| Full Title: Prothrombin complex concentrate in the reduction of blood loss during otrhotopic liver transplantation. | ||||||||||||||||||||||||||||
| Medical condition: liver cirhosis coagulopathy bleeding | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FI (Prematurely Ended) NL (Completed) BE (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2011-000691-34 | Sponsor Protocol Number: ATG-IRA.HVH.10 | Start Date*: 2011-07-06 | ||||||||||||||||
| Sponsor Name:Dra Itxarone Bilbao. Servicio de Cirugía Hepatobiliopancreatica y Trasplantes. HUVH. | ||||||||||||||||||
| Full Title: Single-center pilot study, prospective, open-label, to evaluate the efficacy and safety of immunosuppression low nephrotoxicity, based on the use of ATeGe-Fresenius in patients with renal insuffici... | ||||||||||||||||||
| Medical condition: Renal failure in liver transplantation | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-006870-22 | Sponsor Protocol Number: 1144/2022 | Start Date*: 2022-11-04 | |||||||||||
| Sponsor Name:Medical University of Vienna | |||||||||||||
| Full Title: Substitution of coagulation factors and blood products in patients with liver cirrhosis - A pilot study | |||||||||||||
| Medical condition: Liver cirrhosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003152-43 | Sponsor Protocol Number: DECIPHER-3D | Start Date*: 2016-02-04 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: PILOT STUDY TO EVALUATE THE EFFECTS OF PARITAPREVIR/r, DASABUVIR AND OMBITASVIR ON LIVER FUNCTION AND SYSTEMIC HEMODYNAMIC IN PATIENTS WITH DECOMPENSATED HCV-CIRRHOSIS | |||||||||||||
| Medical condition: PILOT STUDY TO EVALUATE THE EFFECTS OF PARITAPREVIR/r, DASABUVIR AND OMBITASVIR ON LIVER FUNCTION AND SYSTEMIC HEMODYNAMIC IN PATIENTS WITH DECOMPENSATED HCV-CIRRHOSIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002985-70 | Sponsor Protocol Number: MD-R20080507 | Start Date*: 2009-04-23 |
| Sponsor Name:University of Magdeburg | ||
| Full Title: Evaluation of the preventive effect of pentoxifylline and ursodeoxycholic acid to radiation induced liver toxicity after brachytherapy of liver metastases, assessed in a prospective randomised trial. | ||
| Medical condition: Irradiation damage to the liver after HDR-brachytherapy of liver metastases. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
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