Clinical Trials Logo

Cancer clinical trials

View clinical trials related to Cancer.

Filter by:

NCT ID: NCT00952107 Completed - Cancer Clinical Trials

Objective Flap Assessment During Reconstructive Surgery

Start date: June 2009
Phase: Phase 0
Study type: Interventional

The main purpose of this study is to test the ergonomics of an investigational imaging system that can take pictures of blood vessels under the skin. In plastic and reconstructive surgery, blood flow to tissue determines whether the tissue can be transplanted from one location to another. This new imaging device uses invisible near-infrared fluorescent light to see blood vessels that otherwise could not be seen by eye. This study will test the system's basic operation and ergonomics in the operating room.

NCT ID: NCT00948883 Completed - Cancer Clinical Trials

Study of Cancers After Solid Organs Transplants

K-GREF
Start date: October 2008
Phase: N/A
Study type: Observational

About 1500 solid organs transplants are performed each year in the Paris agglomeration. Cancer risk in the transplanted is about three times higher than in a population of the same age without any organ transplant. Thus cancer is an important problem for organ transplant. These cancers can be related to many factors : - Post-transplant cancers are due in part to the non specific immunosuppression, which leads to oncogenic viruses replication, and then produces virus inducted cancers (as lymphoma due to EBV virus). - Post-transplant cancers can also be due to the carcinogenic factors of the immunosuppressive drugs (as cyclosporine or tacrolimus, which can cause the appearance of metastases). However, a new type of immunosuppressive drugs (mTOR inhibitors) appear to have anti-cancer properties. - Post-transplant cancers which are not virus-inducted can be relied to genetic factors of the transplanted patient and/or the transplant donor. There are 4 axes in this study : - Axis 1 : Epidemiological, clinical and biological study of the incident cancers in transplanted patients. - Axis 2 : Qualitative and quantitative immunological study of lymphocyte cells by the transplanted patient (determine their characteristics when a cancer appears). - Axis 3 : Pathological and genetic study of the post-transplant cancer cells (see if the cancer is caused by the donor or the recipient). Creation of a biobank. - Axis 4 : Pharmacogenetic study of the immunosuppressive drugs (determine the impact of patient genetic variability on tolerance and efficiency of the immunosuppressive drugs).

NCT ID: NCT00946803 Completed - Pain Clinical Trials

A Patient-Controlled Cognitive-Behavioral Intervention for Cancer Symptoms

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

Patients receiving treatment for advanced cancer often experience co-occuring pain, fatigue, and sleep disturbance that are not relieved with medications. Brief cognitive-behavioral coping strategies such as relaxation or imagery have been shown to be useful for these symptoms individually and may be effective for the cluster of co-occuring pain, fatigue, and sleep disturbance. Because single cognitive-behavioral strategies don't work equally well for all persons, providing training in multiple cognitive-behavioral strategies is necessary. However, oncology nurses report having insufficient time and are often not available to deliver the interventions exactly when patients experience symptom exacerbation. This application proposes a patient-controlled cognitive-behavioral (PC-CB) intervention, using an MP3 player to deliver recorded cognitive-behavioral strategies. The PC-CB intervention would allow patients to select from a variety of cognitive-behavioral strategies based on their personal preferences, and facilitate self-administration of those strategies at whatever time and place the symptoms occur, without increasing burden on nursing staff. Primary aims are (1) to explore acceptability and patterns of use of the recorded cognitive-behavioral strategies and (2) to pilot test efficacy of the PC-CB intervention compared to a waitlist control.

NCT ID: NCT00942968 Completed - Cancer Clinical Trials

Evaluation of Dalteparin for Long-term (One Year) Treatment of Blood Clots in Subjects With Cancer

Start date: June 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the long term tolerability and safety of dalteparin in subjects with cancer.

NCT ID: NCT00942695 Completed - Cancer Clinical Trials

Energy Value of Macronutrients From Pistachio Nuts and Mechanisms of Nutrient Action

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

The objective of this study is to measure the energy value of pistachios in the human diet and study molecular mechanisms that may help explain the beneficial health effects of pistachios.

NCT ID: NCT00940225 Completed - Cancer Clinical Trials

Study of Cabozantinib (XL184) in Adults With Advanced Malignancies

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

This is a Phase 2 study to evaluate the efficacy and safety of cabozantinib (XL184) in subjects with selected advanced tumor types.

NCT ID: NCT00933855 Completed - Cancer Clinical Trials

Patient Communication Training Intervention

Start date: June 2009
Phase: N/A
Study type: Observational

The purpose of this study is to test a class for Queens Cancer Center patients. We want to find out if patients think this program is helpful.

NCT ID: NCT00932490 Completed - Cancer Clinical Trials

Tailored Intervention Protocol for Oral Chemotherapy Adherence

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

The primary aim of study is to: 1. Test the effectiveness of a tailored protocol in promoting adherence to oral chemotherapeutic agents in adults receiving a new oral chemotherapeutic agent for breast, colorectal, GIST, renal cell,and hepatocellular cancers. Exploratory Aims: 2. Examine adherence to oral chemotherapeutic agents over time at 2, 4 and 6 months in a sample of breast, colorectal, GIST, renal cell,and HPCC cancers patients. 3. Examine the effects of age, gender, caregiver availability, personal involvement in health care, and depression on adherence to oral chemotherapeutic agents.

NCT ID: NCT00930085 Completed - Cancer Clinical Trials

Evaluation of Predictive Proteic Profile on Mortality in the Acute Phase of Septic Shock in Cancer Patients

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

The mortality induced by infections in onco-hematological patients is abnormally high at the acute phase of septic shock. Consequently, it is important to detect the population with a high risk of short term mortality among patients with a septic shock. The aim of this study is the evaluation of predictive proteic profile on the short term mortality in the acute phase of septic shock in cancer patients.

NCT ID: NCT00929058 Completed - Hypertension Clinical Trials

Bevacizumab and Vasoconstriction

BVZ1
Start date: June 2009
Phase: N/A
Study type: Interventional

Rationale: The introduction of angiogenesis inhibitors has remarkably improved treatment of patients with several types of cancer. One of the most common side effects of angiogenesis inhibitors is hypertension. In patients treated with bevacizumab hypertension had an overall incidence up to 32%. The etiology of hypertension caused by treatment with angiogenesis inhibitors is unclear. Objective: To study if arterial bevacizumab infusion causes acute vasoconstriction using plethysmography in healthy volunteers.