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Liver Tumor clinical trials

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NCT ID: NCT02041065 Completed - Liver Tumour Clinical Trials

Waterjet Versus Ultrasound Dissection During Hepatic Transection

Start date: February 2011
Phase: Phase 2
Study type: Interventional

Before liver transection patients are allocated to either waterjet or CUSA to divide the liver parenchyma.

NCT ID: NCT02018107 Completed - Liver Neoplasms Clinical Trials

PET/CT-Assessment of Liver Tumor Ablation

Start date: January 2014
Phase: N/A
Study type: Interventional

In this research study, the investigators are evaluating whether ammonia PET scans or FDG PET perfusion scans are more useful in helping radiologists determine whether liver tumors were successfully destroyed by the heating or freezing procedures (ablations) than other scans currently available to radiologists, such as CT scans and MRI scans. The currently available scan (usually a CT scan with contrast dye) is not always effective in showing how completely the tumor has been destroyed. The ammonia PET scan is a different way of looking at how much tumor has been destroyed. This study will compare the standard scan (CT scan) with the ammonia PET scan.

NCT ID: NCT01819961 Not yet recruiting - Liver Tumor Clinical Trials

Parenteral Fish Oil in Major Laparoscopic Abdominal Surgery

Start date: April 2013
Phase: Phase 4
Study type: Interventional

The aim of this study is to assess the effect of postoperative parenteral fish oil on clinical outcome and immune function after major laparoscopic abdominal surgery.

NCT ID: NCT01812577 Enrolling by invitation - Liver Tumor Clinical Trials

Paravertebral Block for Percutaneous Radiofrequency Ablation of Liver Lesions

TPVB
Start date: December 2012
Phase:
Study type: Observational

Percutaneous radiofrequency ablation of liver lesions causes patients acute pain during and after the procedure. During the procedure patients need deep sedation and cannot be collaborative. Furthermore post-operative analgesia is necessary. The aim of this study is to evaluate if the ultrasound-guided paravertebral block (TPVB)with a single injection can provide anesthesia and post-operative analgesia in these patients.

NCT ID: NCT01782573 Completed - Liver Tumors Clinical Trials

The Efficacy of Chlorhexidine Gluconate Pre - Disinfection Scrubbing in Preventing Surgical Site Infections for Hepatectomy Patients

Start date: October 2011
Phase: Phase 4
Study type: Interventional

To test whether pre - disinfection skin scrub with 4% chlorhexidine gluconate is more effective on the reduction of surgical site microbial colonization and subsequent infection than is normal saline.

NCT ID: NCT01726465 Terminated - Clinical trials for Ischemic Reperfusion Injury

Methylprednisolone N Acetylcysteine in Hepatic Resections

MENHIR
Start date: November 2012
Phase: Phase 2
Study type: Interventional

This is a prospective double-blind randomized phase II clinical trial, with two groups of intervention (one with administration of N-acetylcysteine and the other with administration of methylprednisolone), and one group of placebo. The purpose of this study is to investigate the role of N-acetylcysteine and Methylprednisolone in the modulation of warm ischemia of the liver during hepatic resection. In fact to avoid massive blood loss in liver surgery, continuous or intermittent vascular clamping of the hepatic hilum ('Pringle maneuver') is generally used with good results. However, as a consequence, ischemia and subsequent reperfusion result in complex metabolic, immunological, and microvascular changes, which together might contribute to hepatocellular damage and dysfunction. This phenomenon, known as ischemia-reperfusion (IR) injury of the liver, is a complex multi-path process leading to the activation of some inflammatory pathways. Any patient candidate to liver resection will be enrolled in the study based on the aforementioned criteria. The primary objective of the study is to assess the real efficacy of Methylprednisolone and N-acetylcysteine in reducing the secondary damage from ischemia reperfusion injury in liver resection and in reducing inflammatory response. Secondary objective of the study is whether the reduction of ischemia-reperfusion injury results in: lower incidence of postoperative liver failure, improvement of postoperative liver function, and reduction of blood components transfusions. The randomization will be done the day before the operation. The drugs will be prepared in a blind fashion by the hospital pharmacy. The hospital pharmacy will provide to each patient a drip to make bolus of about an hour before the start of the liver resection and a syringe pump for an infusion of approximately 6 hours. If the patient is enrolled and randomized in the placebo arm, he/she will receive 250 ml of glucose 5% plus the infusion of 100 ml of glucose 5% If the patient is randomized in the Methylprednisolone arm, he/she will receive a dose of 500 mg in 250 ml of glucose 5% plus 100 mg of glucose 5%. If the patient is randomized in the N-acetylcysteine arm, he/she will receive a dose of 150 mg/kg in 250 ml of glucose 5% plus N-acetylcysteine 50 mg/kg in 100 ml glucose 5%. Systematic sampling of liver function tests will be done the day before the operation, at the end of the operation, as well as in postoperative day 1, 3, 5 and 7.

NCT ID: NCT01677728 Recruiting - Colorectal Cancer Clinical Trials

Effect of Target Therapy on Patients Undergoing Synchronic Hepatectomy for Colorectal Liver Metastases

Start date: January 2007
Phase: N/A
Study type: Observational

The aim of this study is to explore whether target therapy in combination with chemotherapy as treatment could improve survival or tumor response in patients undergoing Synchronic Hepatectomy for Colorectal Liver Metastases.

NCT ID: NCT01403727 Completed - Liver Tumors Clinical Trials

Electromagnetic Tracking of Devices During Biopsy Procedures

Start date: November 2011
Phase: N/A
Study type: Observational

The purpose of the trial is to evaluate the differences between PercuNav assisted and unassisted biopsy in the areas of CT radiation dose, procedure time and biopsy accuracy. This prospective, randomized, controlled trial will compare the use of electromagnetic tracking and image guidance (CT) during biopsy procedures verses the typical CT image guided procedure alone.

NCT ID: NCT01197820 Terminated - Liver Tumors Clinical Trials

Hepatic and Renal Thermography Using Magnetic Resonance Imaging

THeR-IRM
Start date: September 2010
Phase: N/A
Study type: Interventional

Several technological challenges exist to apply Magnetic Resonance guided High Intensity Focused Ultrasound (MRgHIFU) for treatment of liver or kidney in particular challenges related to the motion of these organs. This study tests a new software to improve thermometry accuracy in mobile organs in patients with liver or kidney tumors. In the same time, the trajectory of the target in 3D is analyzed.

NCT ID: NCT01082419 Completed - Liver Cirrhosis Clinical Trials

Acoustic Radiation Force Impulse Imaging (ARFI) : a New Technique to Assess Liver Elasticity

NARFI
Start date: April 2010
Phase: N/A
Study type: Interventional

Liver stiffness measurement (LSM) by non invasive methods is increasingly used to estimate liver fibrosis in patients with chronic liver diseases. However, there is growing evidence that fibrosis is not the only determinant of liver stiffness. Indeed inflammation, cholestasis, congestion could also interfere with stiffness measurements. Acoustic radiation force impulse imaging (ARFI) is a new technology to perform real time LSM. Using a standard ultrasonographic probe, it offers elastography with a flexible metering box at variable depth, allowing the examination of specific area.