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Cancer clinical trials

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NCT ID: NCT01576107 Completed - Cancer Clinical Trials

MOTIVACTION - Study

Start date: April 2012
Phase: N/A
Study type: Interventional

Impact of a 4-week exercise intervention vs. a stress-management-training on physical activity (measured objectively and by questionnaire) of cancer patients of different entities and out-patient regimes.

NCT ID: NCT01574196 Completed - Cancer Clinical Trials

Assessment of Cardiac Autonomic Function in Adulthood After Chemotherapy or Radiotherapy in Childhood

SALTO-SNA
Start date: September 2012
Phase: N/A
Study type: Observational

The SALTO-SNA study is an ancillary study of the SALTO study (Suivi À Long Terme en Oncologie des enfants guéris d'un cancer pédiatrique en régions Rhône-Alpes et Auvergne) coordinated by Dr. Claire Berger, pediatric oncologist at the CHU, Saint Etienne. It aims at re-examining, in their initial treatment center, all patients (a cohort of 495 patients alive in 2011), diagnosed between 1987 and 1992, and cured of childhood cancer (except leukemia) in the Rhône-Alpes and Auvergne regions. The rationale for this study is based on the observation that although the survival rate of childhood cancers has now reached 75%, complications of chemotherapy and radiotherapy are high and greatly increase the risk of mortality in later years (estimated to be 14% in the literature). The morbidity risk of chemotherapy and radiotherapy can be quantified by assessing the activity of the intrinsic cardiac autonomic regulation, which represents a powerful predictor of cardiovascular morbidity to the individual.

NCT ID: NCT01567384 Withdrawn - Cancer Clinical Trials

A Phase I Study of OSI-906 in Combination With Pemetrexed in Advanced Solid Tumor Malignancies

Start date: May 2012
Phase: Phase 1
Study type: Interventional

The purpose of the study is to test the safety of an experimental drug called OSI-906 when combined with pemetrexed at different dose levels and to find out the optimal doses of the two drugs that can be given as a combination. Pemetrexed has been widely used for treatment of certain solid organ tumors and is effective and approved for use in treatment of lung cancer and mesothelioma.

NCT ID: NCT01566994 Completed - Cancer Clinical Trials

Comparing Population Cessation Services

Start date: March 2010
Phase: N/A
Study type: Interventional

If the treatment combining Motivation Enhancement, Reduction Counseling, Nicotine Replacement Therapy and Transtheoretical tailored interventions produces an increasing treatment trajectory, it will produce unprecedented impacts with unmotivated smokers specifically and population cessation generally. These recruitment and intervention strategies require limited resources from health care providers and could be readily disseminable to other health care systems for application with populations of smokers, especially unmotivated smokers who have been understudied and underserved.

NCT ID: NCT01565421 Withdrawn - Cancer Clinical Trials

Efficacy Study of Maintenance Therapy for Ovarian Cancer Patients

Start date: September 2008
Phase: Phase 2
Study type: Interventional

This study will assess the effect of IT-101 on delaying cancer progression in patients with platinum sensitive ovarian cancer.

NCT ID: NCT01563679 Completed - Cancer Clinical Trials

Analysis of Percutaneous Ablations for Cancer Treatment

Start date: February 2012
Phase: N/A
Study type: Observational

This is a study involving patients with cancer who are referred by their treating physician for percutaneous locoregional therapies. Patient's clinical and radiology findings, pathology findings, survival, treatment responses, and complications after their locoregional therapy will be studied.

NCT ID: NCT01562626 Suspended - Cancer Clinical Trials

Phase I/II Study of APS001F With Flucytosine and Maltose in Solid Tumors

Start date: September 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test the safety and efficacy of an investigational drug called APS001F when given with flucytosine (5-FC) for treatment of solid tumors. APS001F is a recombinant Bifidobacterium longum (a live bacteria normally found in the digestive tract) that has been modified to produce an enzyme, cytosine deaminase (CD). The patient will first receive an injection of APS001F followed by oral 5-FC. APS001F is expected to go to the site of the tumor(s) where the agent will produce CD enzyme. CD enzyme will convert the 5-FC into 5-fluorouracil (5-FU) which is a standard chemotherapy drug for several types of cancer. Additionally, some patients will also receive 10% maltose injection, a sugar that has been shown to enhance the growth and effectiveness of APS001F in animals. This is the first study where APS001F is being used in humans.

NCT ID: NCT01562067 Not yet recruiting - Cancer Clinical Trials

Sonographic Characteristics of Tumor Indices in Patients With Cervical Cancer During Chemo-radiotherpy

Start date: March 2012
Phase: N/A
Study type: Observational

Cervical tumors are characterized by vascular changes (in terms of quantity, volume and Flows) in the tumor. Due to a good access to the cervix through the vagina, these parameters can be assessed using a three dimensional supersonic. Sonographic characteristics of tumor indices measures before and after oncological treatments may shed light on the patient's prognosis.

NCT ID: NCT01561911 Completed - Cancer Clinical Trials

A Phase I Study of the Chimeric Anti-CD40 Monoclonal Antibody ChiLob 7/4 to Treat Advanced Malignancies Refractory to Conventional Anti-cancer Treatment

Start date: July 2007
Phase: Phase 1
Study type: Interventional

The Purpose of this study is to evaluate the safety and tolerability, and the biological effects of the chimeric anti-CD40 monoclonal antibody Chi Lob 7/4, given intravenously, weekly for 4 weeks in the treatment of patients with advanced malignancies refractory to conventional anti-cancer treatment.

NCT ID: NCT01559883 Completed - Cancer Clinical Trials

Study on Thrombosis Therapy in German Cancer Patients

Start date: February 2012
Phase: N/A
Study type: Observational

The study aims to document the flow of German patients with cancer and acute deep vein thrombosis from first visit to diagnosis and treatment, the applied diagnostic procedures, and therapy modalities.