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Neoplasms, Second Primary clinical trials

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NCT ID: NCT00517803 Completed - HIV Infections Clinical Trials

Micronutrient Supplemented Probiotic Yogurt for HIV/AIDS and Other Immunodeficiencies

Start date: September 7, 2007
Phase: N/A
Study type: Interventional

We hypothesize that micronutrient fortified probiotic yogurt can improve nutritional status and enhance immunity parameters in subjects HIV/AIDS and other immunodeficiencies. We have developed a micronutrient-fortified probiotic yogurt that has safe and beneficial levels of micronutrients for human consumption. This has been undertaken with the guidance of Edward Farnworth, a senior research scientist at Agri-Food Canada-Food Research and Development Centre, St. Hyacinthe, Quebec We will now measure nutritional parameters (height, weight, serum albumin, serum nutrient levels, blood urea, liver function tests (AST, ALT)) to determine if there is a statistically significant difference between the various levels of fortified probiotic yogurt and the placebo on the nutritional parameters of the subjects consuming the yogurt. We will measure immunological parameters (CD4 lymphocyte count, CBC, levels of TNFα, IL-12, IL-10, and G-CSF [Kim, et.al. 2006]) in order to determine if there is a statistically significant difference using fortified probiotic yogurt compared to a placebo. In addition, we will determine if the micronutrient-fortified probiotic yogurt has a significant impact on the overall quality of life for the subjects using the "linear analogue self assessment" tool [Kaiser, et.al 2006].

NCT ID: NCT00440310 Completed - Clinical trials for Colorectal Neoplasms

Phase 3 Trial of Litx™ Plus Chemotherapy vs. Chemotherapy Only Treating Colorectal Cancer Patients With Recurrent Liver Metastases

Start date: February 2007
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the overall survival and progression free survival of patients treated with Litx™ + chemotherapy versus chemotherapy alone in the treatment of Colorectal Cancer with recurrent liver metastases, and to demonstrate the safety of Litx™ therapy. Litx™ consists of a light-activated drug, talaporfin sodium (LS11, Light Sciences Oncology, Bellevue, Washington), and a light generating device, composed of light-emitting diodes (LEDs), that is energized by a power controller and percutaneously placed in the target tumor tissue inside the body.

NCT ID: NCT00437957 Terminated - Brain Metastases Clinical Trials

Phase I Study of Temozolomide, Valproic Acid and Radiation Therapy in Patients With Brain Metastases

Start date: December 2006
Phase: Phase 1
Study type: Interventional

This type of study is called a "Phase I study". Its purpose is to determine the side effects of the two medicines listed in this study when given together with whole brain radiation, and the highest dose of valproic acid that can be given together with temozolomide and whole brain radiation. We will also study the drug combination's effectiveness in treating cancer. While both of these drugs and whole brain radiation have been used in people for many years, they have never been combined for the purpose of treating patients with cancer.

NCT ID: NCT00434317 Completed - Neoplasm Metastasis Clinical Trials

Assessment of Pain and Quality of Life in Breast and Prostate Cancer Patients With Bone Metastases

Start date: August 2005
Phase: Phase 4
Study type: Interventional

This study will evaluate the safety, tolerability and efficacy of zoledronic acid administered intravenously every 3-4 weeks in patients with bone metastases from either breast cancer or prostate cancer.

NCT ID: NCT00406900 Recruiting - Melanoma Clinical Trials

Melanoma Inhibitory Activity (MIA): A Serological Marker for Metastatic Uveal Melanoma

Start date: January 1999
Phase: N/A
Study type: Observational

Uveal Melanoma is the most common primary intraocular tumor in adults. Most tumors metastasize to the liver. So far no sensitive or specific serological tumor marker is routinely used. The marker "Melanoma inhibitory activity" is a promising marker. Study hypothesis is to detect metastatic lesions in an early stage. This would increase life expectance of our patients

NCT ID: NCT00400426 Completed - Clinical trials for Head and Neck Neoplasms

DAHANCA 20 Palliative Radiotherapy for Head and Neck Cancer

Start date: November 2006
Phase: Phase 2
Study type: Interventional

Palliative radiotherapy for head and neck cancer is widely used but the effect and side effects are largely unknown. We will study the effect of short hypofractionated palliative radiotherapy (20 Gy in 4 fractions) on symptom intensity and -frequency as weel as side effects

NCT ID: NCT00374751 Completed - Pain Clinical Trials

Effect of Samarium on the Relief of Pain Due to Vertebral Metastases

Start date: May 2006
Phase: Phase 1/Phase 2
Study type: Interventional

Cancer cells may spread from the primary site to the vertebrae resulting in their deformity. The standard treatment for this case is removal of the cancer deposits in the vertebra and filling the induced cavity with a cement like substance. The investigators are studying the effects (good or bad) of adding samarium (a radioactive substance) to the cement that is injected into the induced cavity.

NCT ID: NCT00334139 Completed - Breast Cancer Clinical Trials

Effect of Zoledronic Acid on Bone Metabolism in Patients With Bone Metastasis and Prostate or Breast Cancer

Start date: May 2006
Phase: Phase 4
Study type: Interventional

Bisphosphonates have been used extensively in the treatment and the prevention of skeletal complications associated with bone metastases in patients with breast cancer and prostate cancer. The purpose of this study is to assess the effect of zoledronic acid patients with prostate cancer or breast cancer and bone metastasis.

NCT ID: NCT00328575 Completed - Neoplasm Metastasis Clinical Trials

Using Intensity Modulated Radiation Therapy (IMRT) for Brain Metastases

Start date: October 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if using intensity modulated radiation therapy for brain metastases is safe and will improve local control more than standard whole brain radiation therapy.

NCT ID: NCT00321620 Completed - Bone Metastases Clinical Trials

Study of Denosumab vs. Zoledronic Acid to Treat Bone Metastases in Men With Hormone-refractory Prostate Cancer

Start date: April 1, 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if denosumab is non-inferior to zoledronic acid (Zometa®) in the treatment of bone metastases in men with hormone-refractory prostate cancer