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Liver Neoplasms clinical trials

View clinical trials related to Liver Neoplasms.

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NCT ID: NCT01929902 Completed - Pancreatectomy Clinical Trials

Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery

Start date: July 2013
Phase:
Study type: Observational

The purpose of this study is to test the efficacy and accuracy of the Aquamantys device.

NCT ID: NCT01924741 Enrolling by invitation - Liver Neoplasms Clinical Trials

Registry of Major Liver Resections Including ALPPS and Other Liver Resections in Two Stages

ALPPSREG
Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

Recently a new method of induce similar hypertrophy in the liver as is observed after hepatectomy has been described and was given the eponym "ALLPS". "ALPPS" stands for Associating Liver Partition with Portal Vein Ligation for Staged Hepatectomy (ALPPS). Since the procedure is used worldwide this international registry was created to enable tracking of cases performed worldwide for safety and outcomes and innovations by the groups involved as well as allows a non-randomized comparison to the conventional methods of portal vein occlusion.

NCT ID: NCT01917370 Active, not recruiting - Clinical trials for Intrahepatic Cholangiocarcinoma

VEGF Signaling Promotes Cell Growth and Metastasis in Intrahepatic Cholangiocarcinoma in a VEGF Receptor Mediated Pathway

icc
Start date: October 2012
Phase: N/A
Study type: Observational

The investigators study the VEGF signaling in ICC cell lines/human tissues and its mechanism in HCC growth, proliferation and apoptosis.

NCT ID: NCT01914289 Recruiting - Clinical trials for Intrahepatic Cholangiocarcinoma

Prognosis of Resection and Radiotherapy in the Treatment of Intrahepatic Cholangiocarcinoma Patients

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to confirm that prognosis of Intrahepatic Cholangiocarcinoma (ICC) with resection and radiotherapy ,to find which is safe and effective treatment.

NCT ID: NCT01908166 Completed - Kidney Tumor Clinical Trials

Ultrasound Elastography in Diagnosing Patients With Kidney or Liver Solid Focal Lesions

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

This clinical trial studies ultrasound elastography in diagnosing patients with kidney or liver solid focal lesions. New diagnostic procedures, such as ultrasound elastography, may be a less invasive way to check for kidney or liver solid focal lesions.

NCT ID: NCT01906021 Completed - Liver Cancer Clinical Trials

Study of New Software Used During Ablations

Start date: September 23, 2013
Phase: N/A
Study type: Interventional

Background: - Ablation is a procedure that heats tumor tissue to a high temperature to destroy it. Doctors perform this procedure by putting a probe in the tumor. This delivers heat to the site. Currently, doctors tell what area is heated by using the probe s manufacturer estimates. These estimates are imprecise. Doctors insert small needles to measure the temperature around the area being heated. Doctors also perform scans of the area, but these cannot show which tissue has been heated and which has not. Right now, only contrast scans can show that. But researchers have developed software that uses images from routine scans to create a temperature map. They want to test the software to see if doctors can monitor the procedure without using more needles and without contrast scans. Objectives: - To test software that might help doctors perform ablations better in the future. Eligibility: - People over 18 years of age already scheduled to have an ablation. Design: - Participants will be screened with a medical history. - Participants will visit the clinic for their already-scheduled ablation. The doctor will use the study software to analyze the temperature in the area being heated. The software will not come into contact with a participant s body. - Participants will undergo scans that are necessary for the procedure, but one or two additional scans may be done as part of this study.

NCT ID: NCT01899261 Completed - Clinical trials for Advanced Adult Hepatocellular Carcinoma

Stereotactic Body Radiation Therapy in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery

Start date: October 7, 2010
Phase: N/A
Study type: Interventional

This pilot clinical trial studies stereotactic body radiation therapy in treating patients with liver cancer that cannot be removed by surgery. Stereotactic radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue.

NCT ID: NCT01895673 Completed - Liver Neoplasms Clinical Trials

PET-MRI After Radiofrequency Ablation (RFA) or Microwave Ablation (MWA)

Start date: June 2013
Phase: N/A
Study type: Observational

The primary objective of this study is to evaluate the ability of PET-MRI and to detect a local site recurrence during the first year of follow-up after RFA or MWA of colorectal liver metastases (CRLM) as compared with contrast enhanced (ce) CT and PET-CT. Standard reference will be clear focal uptake in the rim of the lesion on PET-CT, possibly in combination with histology (when available) or clinical follow-up. Secondary outcomes are the inter-observer variability, the ability to diagnose new intrahepatic lesions and in what way PET-MRI is able to influence future treatment compared to PET-CT and ceCT. The patients satisfaction concerning the PET-MRI will be examined with a questionnaire.

NCT ID: NCT01895010 Recruiting - Nausea Clinical Trials

Acupoint Electric Stimulation Combined With Tropisetron in Preventing and Treating Nausea and Vomiting After TACE

Start date: June 2013
Phase: Phase 2
Study type: Interventional

Observation on acupoint electric stimulation combined with tropisetron in preventing and treating nausea and vomiting and improving the patient's appetite after TACE for primary or metastatic liver cancer patients.

NCT ID: NCT01891552 Completed - Clinical trials for Colon Cancer Liver Metastasis

Observational Study on Second Line Treatment of Liver Metastases With DEBIRI and Cetuximab

TACETUX
Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

- The recently introduced chemoembolization has been considered to be a very attractive new method in terms of response in the treatment of liver metastases from colon cancer carcinoma (LM-CRC). It appears to be particularly useful if carried out with the new embolization materials. - An 80% response rate was reported using TACE with Irinotecan pre-loaded Beads in patients with liver metastases from colon cancer, who had been pretreated with 2 or more lines of chemotherapy. - Since a greater activity was attained by a combination of Cetuximab and Irinotecan versus Cetuximab in monotherapy, the European Agency for the Evaluation of Medicinal Products (EMEA) has granted authorization to the use of Cetuximab in association with irinotecan in the treatment of irinotecan-refractory CRC-LM. - In this study we want to collect data on on time to progression and tolerability using DEBIRI+Cetuximab in LM-CRC