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Neoplasm Metastasis clinical trials

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NCT ID: NCT00265356 Completed - Colorectal Cancer Clinical Trials

Impact of Positron Emission Tomography Imaging Prior to Liver Resection for Colorectal Adenocarcinoma Metastases

PETCAM
Start date: November 2005
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to improve the management of patients with potentially surgically curable colorectal cancer liver metastases. The primary objective is to determine the impact of pre-operative positron emission tomography (PET) on patients who have been assessed as having resectable colorectal cancer liver metastases by conventional imaging (computed tomography (CT) abdomen/thorax, colonoscopy), by determining the proportion of patients who have a change in management resulting from PET.

NCT ID: NCT00264420 Completed - Breast Cancer Clinical Trials

Safety and Efficacy Study of Concomitant Radiotherapy and Zoledronic Acid for Bone Metastases Palliation

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

Zoledronic acid (Zometa) belongs to a class of drugs called bisphosphonates. Bisphosphonates are used in bone metastases to keep the cancerous lesion under control in the bone and to help prevent calcium level elevations in the blood. Cancer cell-culture studies at the Cleveland Clinic showed that zoledronic acid and radiation together have more cell killing effect than either one used alone. The purpose of this study is to monitor the healing of bone lesions when using zoledronic acid together with radiation treatment.

NCT ID: NCT00263588 Completed - Neoplasms, Breast Clinical Trials

Lapatinib for Brain Metastases In ErbB2-Positive Breast Cancer

Start date: December 2, 2005
Phase: Phase 2
Study type: Interventional

Determine how safe and effective lapatinib is when used to treat patients with ErbB2 overexpressing breast cancer that has spread to the brain and is still progressing there even after radiation treatment using WBRT (whole brain radiotherapy) or SRS (stereotactic radiosurgery) to the brain. Lapatinib is an oral drug that will be taken every day. Tests for safety and efficacy will be performed every 4 weeks or 8 weeks (depending on the test) during the course of the study.

NCT ID: NCT00261950 Completed - Clinical trials for Secondary Hyperparathyroidism

Bone Biopsy Study For Dialysis Patients With Secondary Hyperparathyroidism of End Stage Renal Disease

BONAFIDE
Start date: May 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of cinacalcet on markers of bone turnover in patients with kidney disease who are receiving dialysis.

NCT ID: NCT00257855 Completed - Clinical trials for Secondary Progressive Multiple Sclerosis

A Randomised Controlled Trial of Neuroprotection With Lamotrigine in Secondary Progressive Multiple Sclerosis

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

A present there is no safe treatment for reducing rate at which disability worsens in people with secondary progressive multiple sclerosis. Recent research has suggested the possibility that drugs that act by blocking the entry of sodium into nerve cells can protect nerve fibres in the brain and spinal cord. In this trial, the investigators will test whether one such drug, called lamotrigine, can prevent damage to nerve fibres and reduce the rate at which MS worsens. The period of treatment in the trial will run for 2 years.

NCT ID: NCT00255814 Completed - Metastatic Cancer Clinical Trials

Radiation Therapy in Treating Patients With Liver Metastases

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

RATIONALE: Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. PURPOSE: This phase I trial is studying the side effects and best dose of radiation therapy in treating patients with liver metastases.

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: 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.