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Hepatectomy clinical trials

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NCT ID: NCT02548910 Completed - Liver Neoplasms Clinical Trials

Phlebotomy to Prevent Blood Loss in Major Hepatic Resections

PRICE
Start date: April 2016
Phase: N/A
Study type: Interventional

Major liver resection is associated with substantial intraoperative blood loss. Blood loss in elective liver surgery is a significant factor of perioperative morbidity and mortality, as well as possibly long-term oncologic outcome. The purpose of this study is to use whole blood phlebotomy to decrease the central venous pressure, resulting in a state of relative hypovolemia. It is hypothesized that this intervention will lead to a decrease in blood loss at the time of liver resection.

NCT ID: NCT02353702 Completed - Hepatectomy Clinical Trials

Efficacy of Local Anesthesic on Diaphragmatic Function After Upper Abdominal Surgery

CATPAR
Start date: July 2014
Phase: Phase 3
Study type: Interventional

Upper abdominal surgery is known to induce such pulmonary complications as pneumonia, atelectasis, pleural effusion. The post operative diaphragmatic dysfunction participates to these complications and lasts for 7 days after upper abdominal surgery. The sniff-test is a recognized tool for measuring the diaphragmatic function.The purpose of this study is to evaluate the effectiveness of parietal analgesia with continuous infiltration of local anesthesic on diaphragmatic function after upper abdominal surgery through a subcostal incision. Our main outcome is to measure the diaphragmatic function with the sniff test in 44 patients with parietal infiltration of ropivacaine and in 44 patients with placebo. Our secondary outcomes are the evaluation of the effect of continuous parietal analgesia with ropivacaine on IPmax and EPmax, oxygen saturation, post operative pulmonary complications and post operative recovery. This prospective study will determine if the pre peritoneal local infiltration of ropivacaine is useful to decrease post operative diaphragmatic dysfunction.

NCT ID: NCT02056041 Completed - Cirrhosis Clinical Trials

Selection Criteria for Safe Hepatectomy for Hepatocellular Carcinoma

Start date: January 2004
Phase: N/A
Study type: Observational

Selection criteria for safe hepatectomy for HCC are not well established. The aim of this study was the validation of the selection criteria for safe hepatectomy for hepatocellular carcinoma.

NCT ID: NCT02056028 Completed - Hepatectomy Clinical Trials

Bile Leak After Liver Surgery

Start date: January 2004
Phase: N/A
Study type: Observational [Patient Registry]

The definition of biliary fistula is heterogeneous and the more accepted is that proposed by the ISGLS. We devised a precise definition of post-resectional biliary fistula and a well-established policy both for its disclosure and management.Aim was the validation of our definition, and management of biliary fistula after hepatic resection in a large prospective cohort of patients and its comparison with that of the International Study Group of Liver Surgery (ISGLS).

NCT ID: NCT02041871 Completed - Hepatectomy Clinical Trials

Interest of PReOPerative Immunonutrition in Liver Surgery for Cancer

PROPILS
Start date: September 2013
Phase: N/A
Study type: Interventional

To study the efficacy of preoperative immunonutrition in reducing postoperative morbidity after liver resection for cancer.

NCT ID: NCT01950845 Completed - Colorectal Surgery Clinical Trials

Automated Versus Manual Fluid Management for High Risk Abdominal Surgical Patient. A Prospective, Randomized Trial

CL vs CP
Start date: February 2014
Phase: N/A
Study type: Interventional

Dynamic parameters like pulse pressure variation have been shown to be accurate predictors of fluid responsiveness. Hemodynamic optimization based on fluid management and stroke volume optimization have been shown to improve patient outcomes, especially for moderate and high risk abdominal surgical patients. A novel closed-loop fluid administration system based on multi-parameter hemodynamic monitoring have been described recently. This prospective, randomized, surgeon and patient blinded study aims at comparing the cardiac output provided by either this closed-loop system or the anesthesiologist team in high-rish surgical patient elected for abdominal surgery at Pierre Bénite University Hospital, Hospices Civils of Lyon, France. Primary endpoint is the mean indexed cardiac output during surgery per group. We will also compare hemodynamic parameter (cardiac output, stroke volume, blood pressure heart rateā€¦) and patient's outcomes (morbidity, mortality, transfusion rate, hospital length of stay) between groups

NCT ID: NCT01617811 Completed - Hepatectomy Clinical Trials

Effect of Epidural Anesthesia and Analgesia on Patients' Outcomes After Liver Resection

Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to analyze the effects of epidural anesthesia and analgesia on intraoperative clinical outcome, postoperative recovery, metabolic changes, and immune functions of the patients receiving open liver resection.

NCT ID: NCT01469442 Completed - Hepatectomy Clinical Trials

Postoperative Biliary Fistula Prevention After Hepatectomy

Start date: May 2009
Phase: N/A
Study type: Interventional

Aim : Effect of external biliary duct stent after hepatectomy on the occurence of postoperative biliary fistula. Methods : French prospective multicenter randomized trial. Population study: Adult patients who underwent hepatectomy (> 2 segments) on non-cirrhotic liver. Hypothesis: decreased postoperative biliary fistula from 15% to 5% with the presence of a external biliary duct stent. With this hypothesis, the number of patients required to be equal to 152 per group for a total of 304 patients. Outcome measure: Primary : Postoperative biliary complications (biliary fistula, biloma, biliary peritonitis) Secondary : All morbidity, mortality, additional manoeuvres to treat biliary fistula, during of hospital stay and biliary fistula. Follow up: A follow-up of patients 3 months after surgery for all patients. The planned total duration of the study is 3 years and 3 months.

NCT ID: NCT01409499 Completed - Clinical trials for Hepatocellular Carcinoma

Palliative Treatments for Patients With Advanced Hepatocellular Carcinoma (HCC)

2011PTAHCC
Start date: January 2011
Phase: Phase 4
Study type: Interventional

The standard treatment choice for advanced hepatocellular carcinoma (HCC) is sorafenib, and its efficacy is limited. More active treatments were performed in patients with advanced HCC in China, which include radical hepatectomy or TACE. The study is to investigate whether the active treatment will profit survival of patients, and to evaluate the safety.

NCT ID: NCT01223326 Completed - Hepatectomy Clinical Trials

N-acetylcysteine to Reduce Ischemia/Reperfusion Injury in Liver Resection

Start date: January 2003
Phase: Phase 4
Study type: Interventional

Study hypothesis: N-acetylcysteine (NAC) can reduce ischemia/reperfusion injury in liver resection performed under ischemic preconditioning and intermittent portal triad clamping.