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Hepatectomy clinical trials

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NCT ID: NCT01194843 Completed - Pain Clinical Trials

Placebo-controlled Evaluation of Ropivacaine Efficacy by Local Infiltrations

DPO
Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the efficacy and impact on morphine consumption of ropivacaine administered by local per and post hepatic surgery infiltration. Patients will be randomized to either ropivacaine or physiological serum, with equivalent administration modalities in both arms. Patients will be followed during 4 days after the surgery. They will also come back for a follow-up visit one month later. It is necessary to enrol 100 patients. The estimated period of inclusion is 24 months. This is a prospective, comparative, monocentric, double-blind randomized study.

NCT ID: NCT00978757 Completed - Hepatectomy Clinical Trials

The Effect of Ketamine on Interleukin-6 Synthesis in Hepatic Resections Requiring Temporary Porto-arterial Occlusion

Start date: June 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether ketamine is effective to inhibit interleukin 6 synthesis in hepatic resections requiring temporary porto-arterial occlusion.

NCT ID: NCT00966745 Completed - Hepatectomy Clinical Trials

Milrinone During Living Donor Hepatectomy

Start date: January 2008
Phase: N/A
Study type: Interventional

Maintaining a low central venous pressure during living donor hepatectomy is routine practice. The investigators tried to test the hypothesis that using milrinone to maintain a low central venous pressure (CVP) during is associated with a superior surgical field and less blood loss.

NCT ID: NCT00733200 Completed - Cholangiocarcinoma Clinical Trials

Surgical Treatment of Hilar Cholangiocarcinoma: Minor or Major Liver Resection?

Start date: n/a
Phase: N/A
Study type: Interventional

The investigators conducted a prospective study to determine the safety and efficacy of minor and major hepatectomy selected by predetermined criteria in 138 patients with hilar cholangiocarcinoma. In selected patients, minor liver resection was a good treatment.

NCT ID: NCT00730743 Completed - Hepatectomy Clinical Trials

Study on Clinical Outcome of Vascular Inflow Occlusion in Open Liver Resection

Start date: May 2008
Phase: N/A
Study type: Interventional

This study aims to evaluate whether applying inflow vascular occlusion in modern liver resection is associated with better clinical outcome. Eligible patients are randomly assigned to the two surgical techniques: with or without the application of inflow vascular occlusion. Patients outcome including liver function recovery, operative time and blood loss are compared.

NCT ID: NCT00708513 Completed - Hepatectomy Clinical Trials

Intraoperative Cell Saver Autotransfusion Use for Major Surgical Oncology Operations.

Cellsaver
Start date: December 2003
Phase: N/A
Study type: Observational

The purpose of this study is to demonstrate the safety and benefit of auto-transfusion filtered blood in patients undergoing major surgical oncology procedures.

NCT ID: NCT00652587 Completed - Clinical trials for Hepatocellular Carcinoma

Hepatectomy With or Without Transcatheter Arterial Chemoembolization for Stage IIIA Hepatocellular Carcinoma

Start date: January 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether hepatectomy combining with adjuvant transcatheter arterial chemoembolization (TACE) for Stage IIIA hepatocellular carcinoma (HCC) resulting better long-term survival outcome when compared with hepatectomy alone.

NCT ID: NCT00518908 Completed - Hepatectomy Clinical Trials

Organ Protection With Sevoflurane Postconditioning

Start date: January 2008
Phase: N/A
Study type: Interventional

Organ protection, volatile anesthetics, postconditioning, hepatic surgery

NCT ID: NCT00219856 Completed - Hepatectomy Clinical Trials

Effects of Propofol on Oxidative Stress and Liver Regeneration After Partial Hepatectomy

Start date: August 2004
Phase: Phase 3
Study type: Interventional

Propofol is an anaesthetic agent that showed in vitro and in vivo anti oxidant properties. No data are available concerning the potential benefit of a total anaesthesia with propofol in partial hepatic surgery. Patients who undergo partial hepatic resection have frequent liver insufficiency that could be related in part to the oxidative stress induced by clamping the hepatic vessels during the surgical intervention. Our hypothesis is that propofol, by increasing liver resistance to this ischemia-reperfusion phenomenon, could improve the remaining liver function recovery, and therefore could reduce post surgical morbidity. The aim of the study is to evaluate the anti oxidant effects of propofol compared to another widely used anaesthetic agent, inhaled desflurane, during and after partial hepatic resection with hepatic vessels clamping. The primary endpoint will be the level of malondialdehyde (a plasmatic marker of oxidative stress), 30 minutes after the end of hepatic clamping.

NCT ID: NCT00200148 Completed - Hepatectomy Clinical Trials

Acute Normovolemic Hemodilution Versus Standard Intraoperative Management in Patients Having Hepatic Resection and Pancreaticoduodenectomy

Start date: March 2004
Phase: Phase 3
Study type: Interventional

With a major liver or pancreas operation, there is a chance that one will require a transfusion of blood products (either red blood cells or plasma). This may be necessary during the operation or a few days after surgery. The surgeons at Memorial Sloan-Kettering Cancer Center perform a very large number of liver or pancreas resections every year and have pioneered techniques that minimize bleeding during the operation. Even so, liver or pancreas operations such as the one that will be undergone carry a 50% chance of requiring a transfusion. A technique that might lower the need for transfusions is called acute normovolemic hemodilution (ANH). ANH was first introduced over twenty years ago and has been used in many types of operations, including liver or pancreas resection. The studies done on ANH at other hospitals suggest that it may help conserve blood. Researchers at Memorial Sloan-Kettering Cancer Center are conducting a study to determine if ANH is better than the 'standard technique' that is currently used in all patients. The purpose of this study is to find out which of the two techniques is better. The purpose of the study is to see if ANH lowers the need for the transfusion of blood products during and after liver or pancreas resection. The second purpose of the study is to see how ANH changes the length of the operation, the length of time one spends in the hospital, and the complication rate after surgery. The researchers will also see if ANH requires any changes in the administration of anesthesia.