Clinical Trials Logo

Cancer clinical trials

View clinical trials related to Cancer.

Filter by:

NCT ID: NCT00183742 Completed - Cancer Clinical Trials

Trial of Liposomal Doxorubicin (Doxil) and Weekly Docetaxel (Taxotere)

Start date: December 2000
Phase: Phase 1
Study type: Interventional

This study is for patients with advanced cancer that has failed treatment with conventional therapy or for which no standard treatment exists. The purpose of this study is to determine the highest dose that can be given of 2 chemotherapy drugs, docetaxel (also called Taxotere) and liposomal doxorubicin (also called Doxil), when given together and to determine the side effects of this combination. Both Taxotere and Doxil are chemotherapy drugs that can decrease the size of several different tumors. Taxotere is approved by the Food and Drug Administration (FDA) for the treatment of breast and lung cancers, and Doxil is approved for the treatment of ovarian cancer.

NCT ID: NCT00181129 Completed - Cancer Clinical Trials

Fatigue and Cancer Treatment(FACT)- an Exercise Intervention

Start date: September 2002
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled trial is to determine the effects of a nurse-directed, home-based walking exercise program to mitigate fatigue and maintain physical functioning during adjuvant therapy for cancer. The sample will be randomized into exercise (EX) or usual care (UC) groups. The independent study variable is participation in a walking exercise program. Outcomes include: fatigue, sleep disturbance, emotional distress, physical functioning and quality of life. The effects of the walking exercise program will be evaluated using self-report questionnaires administered pre- and post-treatment, patient diaries, and symptoms assessments at defined intervals during adjuvant therapy

NCT ID: NCT00181012 Recruiting - Pain Clinical Trials

Benefit of Lidocaine Perfusion in Cancer Related Visceral Pain Resistant to Morphinics

Start date: May 2005
Phase: Phase 3
Study type: Interventional

This study will evaluate the benefit of lidocaine perfusion in cancer related visceral pain resistant to morphinics. It is an efficacy study in adults and children and a randomized prospective study.

NCT ID: NCT00180869 Completed - Cancer Clinical Trials

Unmodified Versus Leuko-Reduced Allogeneic Red Blood Cells Transfusion in Cancer Patients

Start date: September 1997
Phase: Phase 3
Study type: Interventional

There is evidence to suggest that red blood cell concentrate (RBC) transfusion may have immunomodulatory effects. The aim of this randomized single-center trial is to compare immune responses in patients undergoing cancer surgery and given either an unmodified RBC (UN-RBC) or a leuko-reduced RBC (LR-RBC) transfusion perioperatively.

NCT ID: NCT00180830 Terminated - Cancer Clinical Trials

Glivec Phase II Pediatric Study

Start date: December 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Glivec is effective, in children, adolescents and young adults, in the treatment of malignant disease in which evidence suggests a potential pathogenic role of one or more of the tyrosine kinases known to be inhibited by Glivec.

NCT ID: NCT00179868 Completed - Cancer Clinical Trials

C-Reactive Protein as a Predictor of Stem Cell Transplant Complications

Start date: January 2003
Phase: Phase 2/Phase 3
Study type: Observational

The purpose of this study is to determine if C-Reactive Protein levels are predictive for complications post transplant.

NCT ID: NCT00179855 Recruiting - Cancer Clinical Trials

Extracorporeal Photopheresis for Acute Graft Versus Host Disease

Start date: July 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this research study is to evaluate the safety and feasibility of extracorporeal photopheresis (ECP) in the treatment of steroid-refractory acute graft-versus-host disease (GVHD) in children.

NCT ID: NCT00179829 Completed - Cancer Clinical Trials

WT1 for the Detection of Minimal Residual Disease

Start date: February 1999
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if WT1 is an adequate measurement of minimal residual disease in leukemic patients.

NCT ID: NCT00179790 Completed - Cancer Clinical Trials

Reduced Intensity Transplant Using Extracorporeal Photopheresis

Start date: July 2005
Phase: Phase 1/Phase 2
Study type: Interventional

Stem cell transplantation may be used to cure childhood cancers, and other diseases. Traditionally, stem cell transplants use high doses of chemotherapy and radiation. This regimen may cause significant problems after transplant such as infertility, infection, and graft versus host disease (GVHD). Reduced intensity transplant (RIT) uses medications which weaken the immune system, allowing donor cells to take over. The goal of a RIT is to reduce the risk for complications after transplant. Usually medication is used to weaken the immune system, but there are other options such as extracorporeal photopheresis (ECP) that may be less toxic. ECP is currently used for the treatment of GVHD and certain lymphomas. ECP uses a machine that filters white blood cells from the blood, treats them with ultraviolet (UV) light, and then gives all the cells back to the patient. The patient's immune system becomes weaker, allowing the donor cells to replace those of the patient. Studies involving the use of ECP for conditioning have shown fewer side effects than the use of medications. The primary purpose of this clinical research trial is to evaluate the safety and feasibility of ECP as part of a preparative regimen for RIT in children and young adults.

NCT ID: NCT00178386 Completed - Cancer Clinical Trials

Comparison of Educational Services and Outcomes for Patients Treated for Childhood Cancer

Start date: September 2004
Phase: Phase 1
Study type: Observational

The purpose of the study is to evaluate some educational outcomes of children treated for childhood cancer.