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Gastrointestinal Cancer clinical trials

View clinical trials related to Gastrointestinal Cancer.

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NCT ID: NCT01487343 Completed - Breast Cancer Clinical Trials

Patient Factors Impacting Adherence to Oral Chemotherapy

Start date: November 2011
Phase: N/A
Study type: Observational

The purpose of this study is to identify what makes it easier and what makes it harder to take oral chemotherapy.

NCT ID: NCT01449864 Completed - Clinical trials for Gastrointestinal Cancer

Proton Radiotherapy for Upper Gastrointestinal Malignancies

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

The primary objectives are to determine feasibility and the acute toxicity profile of proton therapy with concurrent continuous infusion 5-FU chemotherapy. Secondary objectives are to determine late toxicities and to generate preliminary data on clinical efficacy.

NCT ID: NCT01423799 Completed - Clinical trials for Gastrointestinal Cancer

Immunonutrition and Quality of Life of Cancer Patients Undergoing Oncological Treatment

Neoimmune
Start date: July 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the health-related quality of life following dietary supplementation with an immunonutrition formulation vs an isocaloric/isoprotein control diet supplement in patients suffering from upper digestive tract neoplasia undergoing oncological treatment.

NCT ID: NCT01422993 Completed - Clinical trials for Gastrointestinal Cancer

Pilot Study of Strength and Balance Training Program for Persons With Oxaliplatin Induced Neuropathy

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

The purpose of this study is to evaluate the effects on strength, balance, and neuropathic symptoms (numbness, tingling, pain, weakness) of a 12 week, bi-weekly, 60 minute, group exercise program designed to improve lower extremity strength and balance with persons with oxaliplatin induced peripheral neuropathy.

NCT ID: NCT01375699 Completed - Breast Cancer Clinical Trials

Doxorubicin With or Without Sildenafil, With Analysis of Cardiac Markers

Start date: August 11, 2011
Phase: Phase 1
Study type: Interventional

Sildenafil increases the therapeutic effect of doxorubicin used as treatment for cancers of solid tumors through both an increase in anti-tumor effects and protection from cardiac toxicity.

NCT ID: NCT01202409 Completed - Clinical trials for Gastrointestinal Cancer

CAPOX in KRAS Wild-Type Advanced Adenocarcinoma of the Small Bowel or Ampulla of Vater

Start date: November 2, 2010
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if panitumumab can help to control advanced cancer of the small bowel or ampulla of Vater. The safety of this drug will also be studied.

NCT ID: NCT01200316 Completed - Clinical trials for Gastrointestinal Cancer

Rocking Motion: Physiologic Effect on the Surgical Stress Response

Start date: February 1, 2012
Phase: Phase 1
Study type: Interventional

After having abdominal surgery, patients often experience a lack of bowel function that can cause nausea, vomiting, abdominal swelling, pain, and/or discomfort. This is known as "post-operative ileus." Patients are usually not allowed to leave the hospital until their doctor is sure that their bowel function has returned. The goal of this clinical research study is to compare using a rocking chair to the standard of care in improving post-operative ileus after abdominal surgery.

NCT ID: NCT01058655 Completed - Clinical trials for Gastrointestinal Cancer

RAD001 and AV-951 in Patients With Refractory, Metastatic Colorectal Cancer

Start date: February 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Research has shown that anti-angiogenic agents can be effective therapies to treat cancer. Anti-angiogenic agents target the blood vessels required for tumors to grow. Vascular endothelial growth factor (VEGF) is one of the cell pathways used for this blood vessel growth. When the investigators interfere with the VEGF pathway, the investigators inhibit this blood vessel growth which is required by tumors. One of the study drugs being used, tivozanib (AV-951), selectively interferes with the VEGF pathway. The second study drug being used, everolimus (RAD001) interferes with the mTOR pathway. The mTOR pathway is another pathway involved in blood vessel and tumor cell growth. By combining these two drugs the investigators hope to slow or reverse tumor cell growth in patients whose tumors have become resistant to other therapies for their disease.

NCT ID: NCT00855452 Completed - Clinical trials for Metastatic Breast Cancer

Activated Allogeneic Lymphocytes for Induction Graft Versus Tumor Effect in Metastatic Solid Tumors

rIL-2(LAK)
Start date: January 2009
Phase: Phase 2
Study type: Interventional

The present protocol is a phase 2 study designed to investigate the potential application of allogeneic cell-mediated immunotherapy in metastatic solid tumors, similarly to the well established graft versus leukemia (GVL) effects, in patients with metastatic solid tumors resistant to conventional treatment modalities. Patients will be eligible to participate in a treatment program based on systemic administration of mismatched lymphocytes activated in vitro with rIL-2 (LAK) followed by rIL-2 inoculation in vivo. This treatment is aiming to induce an anti-tumor effect mediated by the efficient killing activity of the rIL-2 activated cells. Prior to cell infusion patients will receive the conditioning treatment with low dose Cyclophosphamide (Cyc) or Fludarabine with 2 injections of low dose alpha interferon. Cell therapy will be combined with specific anti-tumor monoclonal antibodies if available for the specific disease. Further activation of the anti-tumor activity of alloreactive donor T cells and natural killer (NK) cells will be accomplished by in vivo inoculation of rIL-2, aiming for enhancing the anti-cancer potential of donor-derived effectors cells. Patients will receive one - three cycles of cell therapy, as long as there are no signs of Graft- versus - Host - disease (GVHD) and the malignant disease is controlled.

NCT ID: NCT00849979 Completed - Clinical trials for Gastrointestinal Cancer

Validating M.D. Anderson Symptom Inventory (MDASI-GI) in GI Cancer Patients Under Chemotherapy

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

The goal of this study is to learn more about the symptoms that may occur in patients with GI cancer. The types of GI cancer being studied are cancers of the stomach, liver, pancreas, colon, and rectum. Researchers want to test a newly-designed questionnaire called the M. D. Anderson Symptom Inventory - Gastrointestinal (MDASI-GI) questionnaire.