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Liver Tumor clinical trials

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NCT ID: NCT01031784 Completed - Liver Metastasis Clinical Trials

Radioactive Holmium Microspheres for the Treatment of Liver Metastases

HEPAR
Start date: December 2009
Phase: Phase 1
Study type: Interventional

The HEPAR study is aimed at determining the safety of radioactive holmium containing microspheres for the treatment of tumors in the liver. These microspheres will be administered by infusion in the liver artery using a arterial catheter in the femoral artery.

NCT ID: NCT00960609 Completed - Liver Tumors Clinical Trials

Communicating Veins Between Adjacent Hepatic Veins: an Intra-operative Ultrasound Study

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

The search for communicating veins (CVs) between adjacent hepatic veins (HVs) has drawn its rationale from living donor liver transplantation (LDLT). Parenchymal sparing procedures although HVs are resected suggest that probably their presence is underestimated. Taking profit from new improvements in ultrasound technology the investigators aim to better estimate the rate of CVs in a consecutive series of patients in whom resection of one HV at caval confluence is needed.

NCT ID: NCT00955097 Terminated - Liver Tumors Clinical Trials

Evaluation of Intra-operative Ultrasound Contrast Enhancement in the Evaluation of Liver Tumors

Definity®
Start date: May 2008
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to demonstrate the safety and effectiveness of using an intra-operative ultrasound contrast agent(Definity®) for the identification of known liver tumors.

NCT ID: NCT00942383 Terminated - Liver Tumors Clinical Trials

Freehand Ultrasound Elasticity Imaging in Liver Surgery

IOUS
Start date: September 2007
Phase:
Study type: Observational

The purpose of this study is to investigate the potential for visualizing radiofrequency-induced (RFA) and microwave-induced (MWA) hepatic thermal ablation lesions using a novel, high resolution, and freehand ultrasound elasticity imaging method in human subjects.

NCT ID: NCT00877136 Completed - Clinical trials for Hepatocellular Carcinoma

A Treatment of Unresectable Hepatocellular Carcinoma With TheraSphere®

Start date: February 2009
Phase:
Study type: Observational

This is an interdisciplinary study that falls into the Humanitarian Use Device category. There are no hypotheses to be tested in this treatment protocol. The study has the following objectives: 1. Provide supervised access to treatment with TheraSphere® to eligible patients with primary cancer to the liver who are not surgical resection candidates. 2. Evaluate patient experience and toxicities associated with TheraSphere® treatment. 3. Measure tumor response rates

NCT ID: NCT00845689 Active, not recruiting - Liver Tumors Clinical Trials

Prevention of Liver Damage During Liver Surgery

LTR
Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

Liver damage as a consequnce of ischemia (I) and reperfusion (R) is known to harm the liver and could hence be a critical factor of the postoperative outcome of patients undergoing liver surgery. In order to protect the liver from ischemic damage following interventions such as the Pringle Maneuver, preconditioning has been successfully applied in various animal models as well as in humans. Since ischemia inevitably leads to cell hypoxia and subsequnet release of endogenuous metabolites, the investigators hypothesize that instead of brief periods of ischemia, the exogenuous infusion of purine analogues may also protect against subsequent prolonged periods of ischemia. Moreover, after reperfusion, the antiinflamamtory action of purine ananlogue infusion can further attenuated liver damage.

NCT ID: NCT00828607 Completed - Liver Tumors Clinical Trials

Contrast Enhanced (CE) Ultrasound and CE Computed Tomography or CE Magnetic Resonance Imaging in Liver Masses

Start date: January 2009
Phase: N/A
Study type: Observational

This comparison study is performed to show equivalence of CEUS with CECT or CEMR to diagnose noninvasively focal liver masses. This is a multi-center prospective cohort study of 250 subjects, which will be performed at four institutions in Canada. Subjects with a focal liver mass, measuring at least 2.5 centimeters in maximal diameter, will undergo a conventional baseline sonogram followed by a contrast enhanced ultrasound (CEUS). CEUS will be performed on standard ultrasound scanners with contrast specific imaging capability. The contrast agent used is Definity (Lantheus Medical Imaging, Billerica,MA) All subjects will have either a dedicated hepatic contrast enhanced CT or MR scan within 60 days of the CEUS as per the standard of care in the institution. Anonymized image files from all imaging will be shown independently to two readers, blinded to all clinical and demographic data, who will predict malignancy and diagnosis.

NCT ID: NCT00691691 Recruiting - Liver Tumors Clinical Trials

Stereotactic Body Radiation Therapy (SBRT) in the Treatment of Liver Tumors

Start date: November 2007
Phase: Phase 2
Study type: Interventional

Patients with primary hepato-biliary malignancies or liver metastases from gastrointestinal cancer suffer substantial morbidity and mortality from their hepatic disease. Curative resection is feasible only for selected subgroups of patients. The majority of patients have unresectable and incurable disease. Aggressive arterial and systemic chemotherapy have been used in recent years with improved response and survival. However, a significant number of patients, at least one-third of patients with liver metastases from colorectal cancer and two-third or higher of unresectable hepatobiliary cancer, continue to die of liver failure from progressive disease in the liver. Percutaneous ethanol injections, chemoembolization, cryotherapy and thermal ablation using radiofrequency have been used to treat selected patients with smaller tumors (3-4 cm) in areas away from major blood vessels and the biliary tract. However, most unresectable liver cancers did not fit the criteria for these treatments. Therefore, other regional therapeutic option like external radiation therapy may be considered for local control in the liver or symptom palliation