- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
17 result(s) found for: Hepatectomy.
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EudraCT Number: 2009-017768-18 | Sponsor Protocol Number: 0908127 | Start Date*: 2010-03-19 | ||||||||||||||||
Sponsor Name:CHU Saint-Etienne | ||||||||||||||||||
Full Title: Analgésie par bloc continu du plan transverse de l’abdomen en chirurgie d’exérèse hépatique : efficacité et influence sur la réhabilitation précoce. | ||||||||||||||||||
Medical condition: hepatectomy or segmentectomy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003966-42 | Sponsor Protocol Number: 71691 | Start Date*: 2021-02-16 |
Sponsor Name:Erasmus MC | ||
Full Title: Adjuvant hepatic arterial infusion pump chemotherapy after repeat hepatectomy for patients with recurrent colorectal liver metastases without a history of extrahepatic disease – a phase II study | ||
Medical condition: LIver recurrence after hepatectomy for CRLM. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-006001-35 | Sponsor Protocol Number: PREBOT-II | Start Date*: 2021-10-27 | |||||||||||
Sponsor Name:University Hospital Heidelberg | |||||||||||||
Full Title: Randomized controlled trial of PREoperative injection of BOTulinum toxin into the sphincter of Oddi to reduce bile leakage after hepatic resection PREBOT-II | |||||||||||||
Medical condition: Patients undergoing partial hepatic resection for various underlying diseases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002361-35 | Sponsor Protocol Number: Lidocain1 | Start Date*: 2020-05-06 |
Sponsor Name:region Skåne | ||
Full Title: Intavenous Lidocain and postoperative recovery after liver surgery- a randomized double blinded trial | ||
Medical condition: Patients with liver tumours that have liver surgery performed | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005955-40 | Sponsor Protocol Number: HPB01 | Start Date*: 2009-06-08 |
Sponsor Name:University of Edinburgh [...] | ||
Full Title: Induction of Heme Oxygenase-1: a therapeutic approach to reduce hepatic ischaemia-reperfusion injury in liver surgery | ||
Medical condition: This trial is investigating a new treatment for hepatic ischaemia-reperfusion injury in liver resection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005156-26 | Sponsor Protocol Number: PRIN-SUGAR-2014 | Start Date*: 2015-05-27 |
Sponsor Name:Dr. Enrique Alday | ||
Full Title: Effects of neuromuscular block reversal with sugammadex vs neostigmine on postoperative respiratory outcomes after major abdominal surgery. A randomized controlled trial. | ||
Medical condition: Patients of both sexes proposed for major abdominal surgery under general anesthesia plus epidural | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002007-41 | Sponsor Protocol Number: 200603000 | Start Date*: 2007-08-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ORDINE MAURIZIANO | |||||||||||||
Full Title: A Phase II Clinical Trial of Panitumumab in Combination with Infusional Oxaliplatin and Oral Capecitabine (XELOX) Chemotherapy as 1st line Therapy in Patients with Colorectal Cancer and Advanced Li... | |||||||||||||
Medical condition: Previously untreated Patients with Colorectal Cancer and Advanced Liver Metastases. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001402-18 | Sponsor Protocol Number: CIR-MSC-2014-01 | Start Date*: 2015-05-07 | |||||||||||
Sponsor Name:ALEJANDRA GARCIA BOTELLA | |||||||||||||
Full Title: CD133 + CELL INFUSION IN PATIENTS WITH COLORECTAL LIVER ORIGIN METASTASES GOING TO BE SUBMITTED TO A MAJOR LIVER RESECTION | |||||||||||||
Medical condition: patients with liver metastases from colorectal carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004632-24 | Sponsor Protocol Number: | Start Date*: 2008-02-01 |
Sponsor Name:ARTBC | ||
Full Title: OPTIMAL CONTROL OF LIVER METASTASES WITH INTRAVENOUS CETUXIMAB AND HEPATIC ARTERY INFUSION OF THREE-DRUG CHEMOTHERAPY IN PATIENTS WITH LIVER-ONLY METASTASES FROM COLORECTAL CANCER. A PHASE II TRIAL | ||
Medical condition: The primary objective of the study is to increase by 15% the complete macroscopic resection rate of predominantly liver metastases from metastatic colorectal cancer through combining systemic cetux... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) PT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004505-29 | Sponsor Protocol Number: 2676 | Start Date*: 2008-05-15 | |||||||||||
Sponsor Name:Royal Marsden NHS Trust | |||||||||||||
Full Title: Phase II clinical trial of capecitabine and oxaliplatin plus bevacizumab as neoadjuvant treatment for patients with previously untreated unresectable liver-only metastases from colorectal cancer | |||||||||||||
Medical condition: Metastatic colorectal adenocarcinoma with metastases involving the liver only | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005504-18 | Sponsor Protocol Number: APHP201185 | Start Date*: 2021-05-21 |
Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | ||
Full Title: Lenvatinib in neo-adjuvant and adjuvant therapy for poor-prognosis BCLC A HepatoCellular Carcinoma treated by ablative procedure in a curative intent: multicentre phase 2 therapeutic trial | ||
Medical condition: NA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
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: 2007-007863-26 | Sponsor Protocol Number: MO18725 | Start Date*: 2008-07-02 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A multicentre randomized phase II study to assess the safety and resectability in patients with primarily unresectable liver metastases secondary to colorectal cancer receiving treatment with 5-FU,... | |||||||||||||
Medical condition: Colorectal cancer with initially unresectable liver metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) FR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000845-64 | Sponsor Protocol Number: CCR4085 | Start Date*: 2014-12-17 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: A multicentre randomised phase II study of aflibercept plus chemotherapy in patients with colorectal liver-only metastases deemed to be inoperable or unsuitable for upfront liver resection | |||||||||||||
Medical condition: colorectal cancer with liver metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
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 |
EudraCT Number: 2012-001960-31 | Sponsor Protocol Number: S54348 | Start Date*: 2013-05-03 |
Sponsor Name:UZ Leuven | ||
Full Title: Combined drug Approach to Prevent Ischemia-reperfusion injury during Transplantation of Livers (CAPITL): a first-in-men study | ||
Medical condition: Investigation of the ischemia-reperfusion injury in patients who will undergo a liver transplantation after receiving a drug combination/multifactorial modulation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001271-38 | Sponsor Protocol Number: LT 2004 09 | Start Date*: 2006-06-23 |
Sponsor Name:Our Lady's Hospital for Sick Children | ||
Full Title: Intensified pre-operative chemotherapy and radical surgery for HIGH RISK HEPATOBLASTOMA SIOPEL 4 | ||
Medical condition: Hepatoblastoma | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: IE (Completed) BE (Completed) | ||
Trial results: (No results available) |
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