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Liver Neoplasms clinical trials

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NCT ID: NCT03223818 Recruiting - Liver Cancer Clinical Trials

The Impact of Fast-track Perioperative Program After Liver Resection in Hong Kong Chinese Patients

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

Liver cancer was the third leading cause of cancer death in both sexes in Hong Kong and liver resection remains the mainstay of curative treatment. Post-operative recovery from liver resection has historically been fraught with a high incidence of complications, ranging from 15-48%, and the high incidence of complications leads to prolonged hospital stay, ranging from 9 - 15 days, and increase costs of hospitalization. Recent advancement in the perioperative surgical and anesthetic management of patients undergoing liver resection has led to improvement in these outcomes. The investigators department had previously studied the impact and confirmed the benefit of fast-track peri-operative programs after laparoscopic colorectal surgery. Nevertheless, studies regarding its adoption in liver resection are limited. The investigators group had previously reported, in a retrospective cohort, that successful implementation of ERAS protocol was associated with a significantly shorten hospital stay. However, the peri-operative management in that study incorporated a small proportion of components described in ERAS programs for liver resection and there was no direct comparison with conventional peri-operative program. The aim of this study is to compare the clinical and immunological outcomes of Hong Kong Chinese patients undergoing liver resection for liver cancer with a "conventional" vs a "fast-track" perioperative program.

NCT ID: NCT03223142 Recruiting - Neoplasm Metastasis Clinical Trials

Standardization of Multi-modal Tumor Ablation Therapy System

SMTATS
Start date: July 2017
Phase: N/A
Study type: Interventional

This study will document for the safety and efficacy of image guided multi-mode precision ablation system (the combination of cryoablation and radiofrequency ablation) for the treatment of liver malignant, as well as provide the indicator of antitumor immune response for liver malignant in China.

NCT ID: NCT03215355 Withdrawn - Clinical trials for Primary Liver Cancer

Improving CBCT for Liver IG-SBRT Using Gadoxetate Disodium

Start date: August 2017
Phase: Phase 4
Study type: Interventional

This is a feasibility study requiring only three patients to serve as a proof of concept that gadoxetate disodium (a liver specific contrast agent) can be used to improve images taken just before liver SBRT treatments. The hypothesis of this research is that if gadoxetate disodium improves image quality at the time of treatment, then it can be used for image guided radiotherapy (IGRT). Image guidance is the procedure where the 3D CT image that is used to plan a radiotherapy treatment, is aligned to a 3D image taken just before treatment. The better the alignment, the more accurate the treatment, which is crucial for high dose treatments such as SBRT. This research is important for two main reasons. First, it is much less invasive than the standard of care which involves surgically implanting markers in the liver that can move over time. The benefit to harm ratio for surgery, compared to an injection, is much more dramatic. Furthermore, not all patients are surgical candidates, and therefore in those cases radiation oncologists must prescribed a larger area to treat to ensure that none of the cancerous region is missed. The drawback to this method is the irradiation of more normal tissue than necessary, which although deemed to have a greater benefit than harm, is not ideal. Secondly, this research has strong implications in the field of radiation oncology to move towards patient oriented radiotherapy treatments. If successful, radiation treatment to the liver could be performed in less treatments because of the confidence given to radiation oncologists of the cancer location; knowing exactly the healthy liver regions to avoid.

NCT ID: NCT03213314 Completed - Surgery Clinical Trials

HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies

Hepatica
Start date: September 7, 2017
Phase: N/A
Study type: Interventional

This observational clinical cohort study aims to evaluate the clinical utility of LiverMultiScan in quantifying liver health prior to liver resection or TACE. The results will enable further developments in scanning protocols and software, and clearly define the relevance of applying this technology as part of the pre-operative assessment of the patient being considered for liver resection or TACE.

NCT ID: NCT03195699 Active, not recruiting - Breast Cancer Clinical Trials

Oral STAT3 Inhibitor, TTI-101, in Patients With Advanced Cancers

Start date: November 15, 2017
Phase: Phase 1
Study type: Interventional

Many patients have cancers that have increased activity of a protein called STAT3 that contributes critically to the development and growth of their cancer. Despite our knowledge of STAT3's importance to cancer, scientists and doctors have not developed a drug that targets it and that patients can take to treat their cancer more effectively than treatments that are now available. Tvardi Therapeutics, Incorporated has developed a compound, TTI-101, which can be given by mouth and acts as a direct inhibitor of STAT3. Administration of TTI-101 to mice demonstrated that it blocked growth of cancers of the breast, head and neck, lung, and liver and it was safe when administered at high doses to mice, rats, and dogs. In this application, Tvardi is proposing to further develop TTI-101 for treatment of solid tumors for which the prognosis is dismal. The investigators will determine how safe it is when administered to patients with cancer, determine whether an adequate dose can be administered to patients with cancer that will block STAT3 in their cancer, and determine whether treatment with TTI-101 leads to reduced growth of their cancer.

NCT ID: NCT03184493 Recruiting - Liver Cancer Clinical Trials

Celebrex and Metformin for Postoperative Hepatocellular Carcinoma

XBD
Start date: June 2, 2017
Phase: Phase 3
Study type: Interventional

This prospective trial aims to compare the role of celebrex alone, metformin alone, and celebrex plus metformin in preventing HCC recurrence after hepatic resection.

NCT ID: NCT03183219 Completed - Liver Cancer Clinical Trials

Safety and Efficiency of γδ T Cell Against Liver Cancer

Start date: June 15, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

In this study, effects of γδT cells on human Liver Cancer in combination with tumor reducing surgery, for example, cryosurgery going to be investigated.

NCT ID: NCT03178929 Not yet recruiting - Clinical trials for Primary Liver Cancer

Effect of SAMe Treatment on Recurrence After Radical Treatment of Primary Hepatic Carcinoma

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to explore the effect of SAMe on recurrence after radical treatment of Primary liver cancer.

NCT ID: NCT03175016 Recruiting - Clinical trials for Colon Cancer Liver Metastasis

Irinotecan-Eluting Bead (DEBIRI) for Patients With Liver Metastases From Colorectal Cancer

DEBIRI-CRLM
Start date: June 20, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

This is a multicentre, open labeled, single arm study to determine effectiveness and safety of chemoembolization with Irinotecan-Eluting Bead(DEBIRI) in the treatment of unresectable liver metastases in patients with colorectal cancer after chemotherapy failure.

NCT ID: NCT03171428 Completed - Surgery Clinical Trials

Hepatectomy With or Without the Thoraco-abdominal Approach

Start date: January 1, 2007
Phase: N/A
Study type: Observational

The performance of hepatectomy for liver tumors using the thoraco-abdominal approach (TAA) versus the abdominal approach (AA) is still debated. The aim of the study is the analysis of the perioperative outcome of patients operated with or without the TAA for liver tumors.