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Cancer clinical trials

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NCT ID: NCT00738764 Completed - Cancer Clinical Trials

A Trial of PDL192 in Subjects With Advanced Solid Tumors

Start date: July 2008
Phase: Phase 1
Study type: Interventional

This is a phase 1, multicenter, open-label, dose escalation trial of PDL192 in subjects with advanced solid tumors.

NCT ID: NCT00737230 Completed - Cancer Clinical Trials

Care of Cancer Patients With Bowel Injury Caused by Radiation Therapy to the Pelvis

Start date: April 2007
Phase: N/A
Study type: Interventional

RATIONALE: A step-by-step procedure may help health care practitioners diagnose and treat cancer patients with bowel injury symptoms caused by radiation therapy. PURPOSE: This randomized clinical trial is studying the care of cancer patients with bowel injury caused by radiation therapy to the pelvis.

NCT ID: NCT00735618 Completed - Cancer Clinical Trials

Relaxation and Heart Rate Variability

Start date: June 2008
Phase: N/A
Study type: Interventional

Primary: - To characterize the physiologic changes of the autonomic nervous system, demonstrated by heart rate variability (HRV) high frequency (HF) spectral analysis, before and after a 15 minute, one-time, guided relaxation program for cancer patients. Secondary: - To assess whether change of HRV correlates with subjective feeling for anxiety, based on visual analog scale scores.

NCT ID: NCT00735111 Completed - Cancer Clinical Trials

Do Self-Rated Performance Status Scores Correlate With Health-Care-Provider-Scores?

Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if patients are able to self-rate their physical abilities and how these ratings compare to the ratings of their health-care provider.

NCT ID: NCT00734513 Completed - Clinical trials for Cancer of the GI System-stages II III and IV

Partner-Assisted Emotional Disclosure for GI Cancer

Start date: January 2003
Phase: N/A
Study type: Interventional

The long-range goal of this research is to develop better ways of helping GI cancer patients and their caregivers cope more effectively with the demands of the disease. The study is designed to test the hypothesis that a partner-assisted emotional disclosure intervention will be more effective in enhancing patient' psychological adjustment than a cancer education condition.

NCT ID: NCT00733031 Terminated - Solid Tumors Clinical Trials

Phase I, Open-label, Dose-escalation, Safety and PK Study of AZD6918

Start date: August 2008
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to find out what the maximum tolerated dose is for an experimental drug called AZD6918 based on the side effects experienced by patients with advanced solid malignancies that receive daily AZD6918 alone. It is possible that AZD6918 will be administered twice daily. Then maximum tolerated doses in combination with either gemcitabine or pemetrexed will also be investigated.

NCT ID: NCT00727922 Completed - Cancer Clinical Trials

Protective Effect of Mangafodipir Against Oxaliplatin Neurotoxicity

MnDPDP-K04
Start date: June 2008
Phase: Phase 2
Study type: Interventional

Oxaliplatin is a major antitumor agent but its use is limited by potentially disabling neurotoxicity, characterized by a sensitive defect in the extremities.Mangafodipir is a MRI contrast agent with antioxidant properties. Our previous laboratory works showed that mangafodipir is able to prevent hematologic toxicity of several chemotherapy agents, including oxaliplatin and to increase their antitumor activity. Preliminary clinical data suggested that mangafodipir could prevent oxaliplatin neurotoxicity.The primary purpose of the present study is to assess the protective effect of mangafodipir in patients who have a already moderate oxaliplatin neuropathy and in whom the continuation of this treatment is desirable because of significant antitumor effect.

NCT ID: NCT00726011 Completed - Pain Clinical Trials

Tetrodotoxin Open-label Efficacy and Safety Continuation Study

TEC-006OL
Start date: July 2008
Phase: Phase 3
Study type: Interventional

Different pathophysiologic mechanisms are responsible for the development of chronic pain disorders. Pain pathways are triggered in part by ectopic discharges of voltage-sensitive sodium channels, which are in abundance in both the peripheral and the central nervous systems. Tetrodotoxin (TTX) is a selective blocker of Na+ channels and causes analgesia either by decreasing the propagation of action potentials by Na+ channels and/or by blocking of ectopic discharges associated with chronic pain. TTX is extracted from the puffer fish (fugu). Results from animal pharmacology studies revealed that TTX is a more potent analgesic than standard analgesic agents such as aspirin, morphine or meperidine. At present, the management of severe cancer pain generally includes the use of opiates. This can often result in undesirable side effects, and treatment with this type of medication is not always effective. Because currently available pain-relieving therapy is unsatisfactory for many patients, there is a need for new therapeutic approaches for the management of moderate or severe cancer pain. Recent studies indicate that intramuscular (into a muscle) or subcutaneous (under the skin) injections of tetrodotoxin (TTX) may reduce pain in cancer patients who did not respond to standard therapies. The current proposed study (TEC-006OL) is designed to provide the option for all patients who participated in the TEC-006 study (both tetrodotoxin and placebo-treated) to receive or continue to receive tetrodotoxin treatment.

NCT ID: NCT00725114 Completed - Pain Clinical Trials

Safety & Efficacy Study of Subcutaneous Tetrodotoxin for Moderate to Severe Inadequately Controlled Cancer-related Pain

TEC-006
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Different pathophysiologic mechanisms are responsible for the development of chronic pain disorders. Pain pathways are triggered in part by ectopic discharges of voltage-sensitive sodium channels, which are in abundance in both the peripheral and the central nervous systems. Tetrodotoxin (TTX) is a selective blocker of Na+ channels and causes analgesia either by decreasing the propagation of action potentials by Na+ channels and/or by blocking of ectopic discharges associated with chronic pain. TTX is extracted from the puffer fish (fugu). Results from animal pharmacology studies revealed that TTX is a more potent analgesic than standard analgesic agents such as aspirin, morphine or meperidine. At present, the management of severe cancer pain generally includes the use of opiates. This can often result in undesirable side effects, and treatment with this type of medication is not always effective. Because currently available pain-relieving therapy is unsatisfactory for many patients, there is a need for new therapeutic approaches for the management of moderate or severe cancer pain. Recent studies indicate that intramuscular (into a muscle) or subcutaneous (under the skin) injections of tetrodotoxin (TTX) may reduce pain in cancer patients who did not respond to standard therapies. The current proposed study (TEC-006) is designed to 1) demonstrate in a double-blind, placebo-controlled trial that the subcutaneous 30 μg b.i.d. dose of TTX for 4 days is effective in reducing pain outcome and improving quality of life; 2) characterize the onset and duration of analgesia, and 3) demonstrate that TTX is well tolerated in patients with inadequately controlled cancer-related pain.

NCT ID: NCT00724100 Terminated - Cancer Clinical Trials

A Trial of ALB 109564(a) in Subjects With Advanced Solid Tumors

Start date: September 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose of ALB 109564(a), a novel tubulin inhibitor, and to assess safety, pharmacokinetics, and anti-tumor activity in subjects with advanced solid tumors.