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NCT ID: NCT01002560 Recruiting - Malignant Melanoma Clinical Trials

The Identification of Novel Prognostic Markers in Melanoma

Start date: December 2008
Phase: N/A
Study type: Observational

The purpose of this project is to analyze tumour tissue from a group of subjects with malignant melanoma, who have been treated at the Royal Marsden Hospital.

NCT ID: NCT01000129 Recruiting - Bladder Cancer Clinical Trials

Adaptive Planning in Bladder Cancer

APPLY
Start date: January 2009
Phase: Phase 2
Study type: Interventional

To demonstrate that radiotherapy treatments for bladder cancer can be delivered with greater accuracy using a new planning method and that this method can be used simply and effectively by those delivering treatment.

NCT ID: NCT00997464 Recruiting - Prostate Cancer Clinical Trials

An Exploration of Genetic Testing for Prostate Cancer Susceptibility

Start date: August 2009
Phase: N/A
Study type: Observational

Study of the factors that affect interest in - and uptake of - genetic testing for variants that predispose to prostate cancer from the perspective of the patient.

NCT ID: NCT00994617 Recruiting - Clinical trials for Essential Hypertension

Monotherapy Versus Dual Therapy for Initial Treatment for Hypertension

Pathway 1
Start date: January 2010
Phase: Phase 4
Study type: Interventional

To test whether the current custom of initiating treatment for hypertension with a single drug is less effective in the short-term than initial combination therapy, and results in the eventual need for comparatively more antihypertensive drug therapy.

NCT ID: NCT00994552 Recruiting - COPD Clinical Trials

Comparison of Pressure Support and Pressure Control Ventilation in Chronic Respiratory Failure

Start date: August 2009
Phase: Phase 4
Study type: Interventional

This study is looking at whether there is a difference in outcomes using two different types of breathing support in those patients who have chronic respiratory failure (patients who under-breathe). There is little data to demonstrate which mode of ventilation is better in terms of physiological outcomes and outcome data relating to patient symptoms. We hypothesize that one type of breathing support: pressure support ventilation would be more comfortable for patients as it more closely matches a patient's own respiratory pattern and and so leads to improved adherence and consequent improvement in quality of life. Patients with respiratory failure will be randomly assigned to receive either pressure support ventilation or pressure control ventilation for the first 6 weeks and then cross-over to receive the mode not previously used for a further 6 weeks. They will have baseline data recorded and then be followed up after each 6 week block.

NCT ID: NCT00989508 Recruiting - Cardiac Output, Low Clinical Trials

Myocardial Protection With Perhexiline in Left Ventricular Hypertrophy

HYPER
Start date: October 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Open-heart surgery causes injury of the heart muscle. Although this is usually mild, temporary and reversible, if it is severe it can endanger life and require additional high cost care. During surgery, techniques are used to protect the heart from injury, but these remain imperfect. Patients with a thickened wall of the heart (left ventricular hypertrophy) may be at greater risk. This study assesses the effect of facilitating sugar metabolism (a more efficient fuel) by the heart muscle using the drug Perhexiline given before the operation. This treatment has a sound experimental basis for improving outcome. If this improvement is confirmed surgical results could be improved. The investigators will be studying heart function, heart muscle energy stores and chemicals which quantify the amount of heart muscle injury. The investigators' hypothesis is that Perhexiline will improve the protection of the heart by decreasing damage that may occur during heart surgery.

NCT ID: NCT00988130 Recruiting - Prostate Cancer Clinical Trials

High-Intensity Focused Ultrasound Focal Ablation in Treating Patients With Progressive Prostate Cancer

Start date: July 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: High-intensity focused ultrasound focal ablation uses high-energy sound waves to kill tumor cells. PURPOSE: This phase II trial is studying the side effects of high-intensity focused ultrasound focal ablation and to see how well it works in treating patients with progressive prostate cancer.

NCT ID: NCT00987675 Recruiting - Prostate Cancer Clinical Trials

High-Intensity Focused Ultrasound Ablation in Treating Patients With Progressive Prostate Cancer

Start date: July 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: High-intensity focused ultrasound ablation uses high-energy sound waves to kill tumor cells. PURPOSE: This phase II trial is studying the side effects of high-intensity focused ultrasound ablation and to see how well it works in treating patients with progressive prostate cancer.

NCT ID: NCT00986557 Recruiting - Clinical trials for Graft Versus Host Disease

T-Lymphocyte Infusion or Standard Therapy in Treating Patients at Risk of Cytomegalovirus Infection After a Donor Stem Cell Transplant

Start date: September 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: An infusion of cytomegalovirus-specific T lymphocytes may prevent or reduce cytomegalovirus infection during the first year after a donor stem cell transplant. PURPOSE: This randomized phase II trial is studying T-lymphocyte infusion to see how well it works compared with standard therapy in treating patients at risk of cytomegalovirus infection after a donor stem cell transplant.

NCT ID: NCT00982306 Recruiting - Alcoholism Clinical Trials

Brief Interventions in General Hospital (BIG)

BIG
Start date: February 2010
Phase: Phase 1
Study type: Interventional

Alcohol abuse is a widespread concern internationally with a significant threat to world health. Research suggests a relationship between heavy drinking and certain clinical presentations such as injuries, physical and psychiatric illnesses and frequent sickness absence from employment. This research aims to establish whether brief interventions delivered to harmful and hazardous alcohol drinkers admitted to hospital impacts of their alcohol consumption levels on discharge from hospital.