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Neoplasms, Second Primary clinical trials

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NCT ID: NCT00278993 Completed - Prostate Cancer Clinical Trials

Evaluating E7389 in Patients With Hormone Refractory Prostate Cancer With Advanced and/or Metastatic Disease Stratified by Prior Chemotherapy

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

This is a multi-centre, phase II, open-label, two-stage design, single-arm study in patients with hormone-refractory prostate cancer (HRPC) with advanced (rising PSA) and/or metastatic disease and who have had prior anti-androgen therapy. The study will further explore the efficacy of E7389 by enrollment of patients into two strata: those who have had no prior systemic chemotherapy for their disease (except for mitoxantrone and estramustine), and those who failed no more than one previous chemotherapeutic regimen with tubulin-binding agents such as docetaxel.

NCT ID: NCT00265200 Terminated - Metastases Clinical Trials

Using TRAP to Evaluate the Effect of Zometa on Bone Metastasis Due to Lung Cancer

Start date: February 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate a new blood test as a way to follow the effect of Zometa in treating bone metastases due to lung cancer.

NCT ID: NCT00264979 Terminated - Colorectal Cancer Clinical Trials

Evaluation of 2 Resection Strategies of Synchronous Colorectal Cancer Metastases

METASYNC
Start date: March 2, 2006
Phase: N/A
Study type: Interventional

The surgical strategy for the treatment of synchronous colorectal cancer liver metastases has not still been defined. The purpose of this study is to compare two treatment strategies in which liver resection is performed either during, or 12 to 14 weeks after the primary resection. Endpoints include the rate of severe complications and survival.

NCT ID: NCT00244868 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Computer-Based Survey and Communication Aid in Improving Physician-Patient Communication and Treatment Decision Making in Patients With Metastatic Cancer

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

RATIONALE: A computer-based survey and communication aid may help physicians and patients to communicate better and help make treatment decisions easier. PURPOSE: This phase III randomized clinical trial is studying how well giving a computer-based survey together with a communication aid works compared to a computer-based survey alone in improving physician-patient communication and treatment decision making in patients with metastatic cancer.

NCT ID: NCT00241111 Completed - Clinical trials for Prostate Cancer With Bone Metastasis

Assessment of the Efficacy, Tolerability and Pharmaco-economic Impact of Zoledronic Acid Treatment in Prostate Cancer With Bone Metastasis

Start date: September 2003
Phase: Phase 4
Study type: Interventional

Study to determine effectiveness and safety of zoledronic acid and whether it has a pharmaco-economic impact in prostate cancer with bone metastasis.

NCT ID: NCT00219297 Completed - Clinical trials for Non-small Cell Lung Cancer

Study of Patupilone in Patients With Brain Metastasis From Non-small Cell Lung Cancer

Start date: November 16, 2005
Phase: Phase 2
Study type: Interventional

The study objective is to evaluate the safety and efficacy of patupilone with respect to early progression and response of patients with non-small cell lung cancer (NSCLC) metastatic to the brain, who have progressed after chemotherapy, surgery and/or radiation.

NCT ID: NCT00199173 Completed - Colorectal Neoplasm Clinical Trials

Comparing Hepatic Intra-arterial Injection of Yttrium-90 Microspheres Versus Fluorouracil (5FU) in Colorectal Cancer Metastatic to the Liver Only

Start date: n/a
Phase: Phase 3
Study type: Interventional

This is a Phase III trial comparing hepatic intra-arterial injection of Yttrium-90 microspheres (selective internal radiation [SIR] spheres) versus infusional intravenous (IV) 5FU in colorectal cancer metastatic to the liver only and refractory to standard IV chemotherapy.

NCT ID: NCT00172003 Completed - Neoplasm Metastasis Clinical Trials

Effect of Zoledronic Acid in Patients With Renal Cell Cancer and Bone Metastasis

Start date: September 2004
Phase: Phase 4
Study type: Interventional

It is the aim of this clinical study to evaluate the skeletal-related event rate under therapy with zoledronic acid in patients with renal cell cancer having at least one cancer-related bone lesion.

NCT ID: NCT00169845 Completed - Neoplasms Clinical Trials

Beta-carotene and Alpha-tocopherol Chemoprevention of Second Primary Malignancies in Head and Neck Cancer Patients

Start date: October 1994
Phase: Phase 3
Study type: Interventional

Epidemiologic studies suggest that low dietary intakes and low plasma concentrations of antioxidant vitamins and minerals are associated with increased risks of cancer, especially for epidermoid tumors. Patients with stage I or II head and neck cancer have a good prognosis, with a 5-year relative survival of 60% to 90%, depending of the tumor site. However, the benefit of treatment is often compromised by the occurrence of second primary cancers, which develop in 20% of patients during the first 5 years after diagnosis. We conducted a randomized chemoprevention trial among patients with head and neck cancer treated by radiation therapy to determine whether supplementation combining two antioxidants, alpha-tocopherol and beta-carotene, could reduce the incidence of second primary cancers in this patient population (primary objective of the trial). This study was conducted with funds from the NCIC (#008176,004738,013211) and was completed. In this cohort of head and neck cancer patients, we evaluated whether nine potential prognostic serum markers measured at the time of diagnosis were related to recurrence, occurence of second primary cancers and survival. This study was conducted with funds from the NCIC (#018100) and was completed. Presently, we evaluate genetic polymorphisms(GWAS) associated with prognosis (NCIC grant #019502). We also assess the relationship between vitamin D (dietary intake, serum level, and genetic polymorphisms of key vitamin D-related genes) and head and neck long-term outcomes (NCI grant #1R03CA141615-01).

NCT ID: NCT00166686 Withdrawn - Clinical trials for Treatment-Related Cancer

Clonidine for Neurocognitive Sequelae

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

The goals of the study are to determine the efficacy of clonidine in the treatment of children with neurocognitive sequelae following the therapy of long term malignancies. In addition, the study hopes to determine the long-term effect of clonidine on children's academic and psychosocial function.