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Carcinoma clinical trials

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NCT ID: NCT00829335 Completed - Clinical trials for Hepatocellular Carcinoma

Anatomical Resection of the Liver for Hepatocellular Carcinoma: a New Ultrasound Guided Approach

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

Anatomical resection is the gold standard approach for liver resection in patients with HCC. A new method for that by means of IOUS-guided finger compression has been devised.

NCT ID: NCT00827723 Completed - Clinical trials for Carcinoma, Hepatocellular

Indocyanine Green and Portal Pressure in Viral and Alcoholic Cirrhotic Patients With Hepatocarcinoma

Start date: February 2009
Phase:
Study type: Observational

The aim of the investigators' study is to elucidate the relationship between a functional liver test (e.g., ICG) and the PREOPERATIVE value of portal hypertension in the patients with impaired liver function from alcoholic and non-alcoholic aetiologies. Alcoholic and viral cirrhosis present important differences in terms of cellular mechanisms responsible for the disease progression with a distinct and unique gene expression pattern that regulates the type of inflammatory response. These differences probably influence the hepatic functional reserve and the onset of portal hypertension at a comparable clinical and biological level of derangement and the investigators may expect significant differences in the recovery from hepatectomy. The investigators' hypothesis is that at a comparable ICGR-15 rate non-viral cirrhotic liver presents higher portal pressure values and the investigators also argue that alcoholic cirrhotic patients would tolerate a larger hepatic resection than would viral cirrhotic do.

NCT ID: NCT00827554 Completed - Clinical trials for Hepatocellular Carcinoma

The Role of Low Molecular Weight Heparins in Hepatocellular Carcinoma

Start date: December 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Hepatocellular carcinoma (HCC) is a major tumor type worldwide, especially in China as the sequence of hepatitis B and liver cirrhosis. Activation of the coagulation system occurs commonly in patients with malignancy. Several studies have suggested that anticoagulant therapy may improve survival in patients with malignancy. The low molecular weight heparins (LMWHs) lend themselves to such studies because of their effects in experimental models of malignancy and the relative ease of administration compared with unfractionated heparin. The purpose of the present RCT was to determine whether addition of LMWH to transarterial chemoembolization (TACE) would improve HCC patient outcome compared with TACE alone.

NCT ID: NCT00827359 Completed - Clinical trials for Renal Cell Carcinoma

Biomarker Trial of Everolimus in Patients With Advanced Renal Cell Carcinoma

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if certain features of tumor specimens sampled prior to therapy can predict for the likelihood of responding to everolimus.

NCT ID: NCT00827047 Completed - Clinical trials for Hepatocellular Carcinoma

Total Hemihepatic Vascular Exclusion in Hepatectomy in Hepatocellular Carcinoma Treatment

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

Total hemihepatic vascular exclusion(THHVE),completely isolates the right or left hemiliver ipsilateral to the lesion that requires resection from the systemic circulation,has the advantage of preventing backflow hemorrhage or air embolism without having to resort to caval blood flow interruption of THVE.This study is to evaluate if THHVE can raduce bleeding,reduce the incidence of complications and improve the patient's free survival and overall survival compared with hemihepatic vascular clamping and Pringle maneuver.

NCT ID: NCT00826384 Completed - Clinical trials for Hepatocellular Carcinoma

Transarterial Chemoembolization (TACE) Therapy of Hepatocellular Carcinoma (HCC) With Blocking Tumor Blood Temporarily and Enhancing Perfusion

Start date: October 2008
Phase: Phase 1/Phase 2
Study type: Interventional

According to radiology imaging, the patients of HCC are divided into two groups(hypovascular tumor group and moderately vascular tumor group). Every group is divided into TACE therapy with balloon catheter subgroup and regular TACE therapy subgroup. Patients take the TACE therapy each 45 days, and have MRI diffusion examine or CT one week before next therapy. All objects are observed until the end event happening or in the group for 6 months.

NCT ID: NCT00825669 Completed - Clinical trials for Hepatocellular Carcinoma

Treatment of Portal Vein Tumor Thrombus After Hepatocellular Carcinoma Resection

Start date: December 2008
Phase: N/A
Study type: Interventional

Hepatectomy is still the treatment of choice for hepatocellular carcinoma. Part of the patients may present portal vein tumor thrombus (PVTT) after resection. PVTT might lead to upper gastrointestinal bleeding and worsening of hypersplenism which will endanger the life of the patients. PVTT also plays the centre role of recurrence and metastasis of HCC. There is no standard treatment for PVTT yet. We aim to compare the effects of TACE and TACE plus laser ablation for treating patients with PVTT.

NCT ID: NCT00825474 Completed - Clinical trials for Hepatocellular Carcinoma

A Prospective Randomized Trial Comparing Partial Hepatectomy and TACE Plus PEI for Small Hepatocellular Carcinoma

Start date: August 2008
Phase: N/A
Study type: Interventional

Presently,the diagnostic method of small hepatocellular carcinoma has been greatly elevated in China.The treatment is being from simplification to diversification,from entirety to individualization.Confronting small hepatocellular carcinoma,we not select simple operation treatment but select a treatment that have more predominance and more fitting with patients in various kinds of treatment methods;including operation ,TACE,PEI,et al.which is better ? There are many arguments.

NCT ID: NCT00822809 Completed - Cancer Clinical Trials

CASIMAS: Catumaxomab Safety Phase IIIb Study With Intraperitoneal Infusion in Patients With Malignant Ascites Due to Epithelial Cancers

CASIMAS
Start date: December 2008
Phase: Phase 3
Study type: Interventional

This is a randomized phase IIIb study investigating the treatment of malignant ascites due to epithelial cancer (carcinomas) with the trifunctional antibody catumaxomab. In order to make the catumaxomab treatment more convenient for the patient and the hospital praxis the tolerability of 3 hour infusions of catumaxomab with and without premedication of prednisolone is evaluated. A total of 208 patients with malignant ascites due to epithelial cancer will be allocated to two treatment groups in a 1:1 ratio.

NCT ID: NCT00820898 Completed - Clinical trials for Endometrial Adenocarcinoma

Gemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer

Start date: February 2009
Phase: Phase 2
Study type: Interventional

This phase II trial is studying the side effects of gemcitabine and to see how well it works in treating patients with recurrent or persistent endometrial cancer. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.