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Neoplasm Metastasis clinical trials

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NCT ID: NCT00253331 Completed - Raynaud Disease Clinical Trials

Lab Study of MQX-503 in Treatment of Raynaud's

Start date: November 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine, in comparison to a placebo control, the response to two dosage strengths of a topical gel formulation of nitroglycerin, MQX-303, in the determination of finger blood flow and skin temperature in the fingers of patients with moderate to severe Raynaud's phenomenon, follwoing exposure to cold temperatures. Blood flow is determined by scanning laser Doppler equipment and skin temperature is measured using attached thermistor probes. Following baseline measurements, the study gel is applied, the hand is placed in a cold chamber, and then blood flow and skin temperature are monitored for the next two hours. Each patient will receive multiple doses on different days so that each can serve as his/her own control in interpreting the response.

NCT ID: NCT00247403 Withdrawn - Neoplasm Metastasis Clinical Trials

Safety Study of 2DG With Stereotactic Radiosurgery

Start date: October 2005
Phase: Phase 1
Study type: Interventional

Ionizing radiation produces cancer cell death by creating high levels of reactive oxygen species (ROS), such as superoxide and hydrogen peroxide, in irradiated cells. Cancer cells are preferentially affected by ROS. The investigators, therefore, propose that interfering with the detoxification of ROS will make radiation more toxic to cancer cells. Several cellular mechanisms exist to detoxify ROS, and glucose metabolism plays an important role in many of these mechanisms. The investigators propose that interfering with glucose metabolism will sensitize cancer cells to radiation. The investigators' central hypothesis is that 2DG will sensitize cancer cells to ionizing radiation by inhibiting the use of glucose to detoxify reactive oxygen species produced by radiation. As an initial step to evaluate this hypothesis, the investigators have designed this phase I study.

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: NCT00242554 Completed - Prostate Cancer Clinical Trials

Open-label Phase IV Clinical Trial to Evaluate the Safety and Tolerability of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastases

Start date: October 2002
Phase: Phase 4
Study type: Interventional

To assess the effects of i.v. zoledronic acid 4 mg with respect to safety and tolerability

NCT ID: NCT00242086 Completed - Colorectal Cancer Clinical Trials

Comparison of Triphasic CT, PET and MR Tumour With Pathological Findings in Colorectal Cancer Liver Metastases

Start date: October 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to correlate the MRI CT and PET appearances of colorectal liver metastases to pathologic appearance ot better understand the accuracy of imaging to determine tumor size.

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: NCT00238251 Completed - Lung Cancer Clinical Trials

Radiation Therapy Combined With Either Gefitinib or Temozolomide in Pats With NSCLC and Brain Metastases

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

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Gefitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving radiation therapy together with either gefitinib or temozolomide may kill more tumor cells. PURPOSE: This randomized phase II trial is studying how well giving radiation therapy together with either gefitinib or temozolomide works in treating patients with non-small cell lung cancer and brain metastases.

NCT ID: NCT00237159 Completed - Clinical trials for Prostate Cancer Patients With Bone Metastasis

Effect of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastasis

Start date: October 2002
Phase: Phase 4
Study type: Interventional

It is the aim of this clinical study to evaluate the skeletal-related event rate and tolerability of zoledronic acid in patients with prostate cancer patients and bone metastases.

NCT ID: NCT00237146 Completed - Prostate Cancer Clinical Trials

Study to Evaluate Zoledronic Acid on Quality of Life and Skeletal-related Events as Adjuvant Treatment in Patients With Hormone-naïve Prostate Cancer and Bone Metastasis Who Have Undergone Orchiectomy

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

An open, multicenter and prospective study to evaluate the impact of the treatment with zoledronic acid 4 mg, on the quality of life and the skeletal-related events in patients with prostate cancer and bone metastasis that responds to hormonal therapy. Zoledronic acid is given to patients in a 15 minute-infusion every 4 weeks until a skeletal-related event occurs.

NCT ID: NCT00232726 Completed - Neoplasm Metastasis Clinical Trials

Clinical Study of Previously Untreated Patients With Malignant Melanoma

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

Previously untreated patients with malignant melanoma receive a new chemotherapy drug currently under development. CP-4055 is given intravenously on days 1-5 every four weeks until complete response or disease progression.