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The IDEAL Study: a clinical trial of the timing of kidney dialysis initiation on survival in subjects with chronic kidney disease.
Expand descriptionIt has been suggested that dialysis should be commenced early, in subjects with progressive chronic kidney disease, in order to prevent illness and complications however this had never been proven. The IDEAL study was designed to determine when is the best time to commence kidney dialysis for the very first time. 8 Centers are participating in New Zealand. 24 Centers are participating in Australia.
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The effect of a combined aerobic and resistance exercise program on people with Type 2 diabetes and peripheral neuropathy
Expand descriptionThis research aims to investigate the effects of a combined aerobic and resistance exercise program on measures of strength, function and sensation in those with Type 2 diabetes and peripheral neuropathy. It will also aim to explore the safe prescription of exercise for these individuals, its effects on levels of quality of life, and to identify the potential barriers and enablers to a sustained exercise program.
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A double-blind, randomised, multiple dose, phase III, multicentre study of Alpharadin in the treatment of patients with symptomatic hormone refractory prostate cancer with skeletal metastases
Expand descriptionAlsympca is an international Phase III clinical study to evaluate the efficacy and safety of Radium-223 dichloride in patients with hormone refractory prostate cancer and skeletal metastases. The aim of the study is to compare, in patients with symptomatic HRPC and skeletal metastases, the efficacy of best standard of care plus Radium-223 dichloride versus best standard of care plus placebo, with the primary efficacy endpoint being overall survival (OS). Patients will be randomised in a 2:1 allocation ratio (Radium-223 dichloride:Placebo). The study treatment consists of 6 intravenous administrations of Radium-223 dichloride or placebo (saline) each separated by an interval of 4 weeks. The patient will be followed until 3 years after first study drug administration. Within the U.S., the trial is conducted under an IND sponsored by Bayer HealthCare Pharmaceuticals. All patients received BSoC (Best Standard of Care)
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Effect of three different breakfast meals with varying glycaemic load and dairy composition on cognition and satiety in healthy children
Expand descriptionThe aim of the study is to examine the effect of dairy consumption on satiety and certain aspects of cognition (speed of processing, short term memory, working memory, attention and speed of reasoning) in a sample of primary school children aged 10-12 years. Primary outcome measures are post prandial glucose levels, satiety and cognitive functioning. It is hypothesized that meals with a lower glycaemic load and higher dairy composition will be associated with improvements in measures of cognitive function and satiety compared to a meal high in glycaemic load and containing no dairy food.
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Optimising regulatory T cell depletion with cyclophosphamide in combination with chemotherapy for enhanced anti-tumour immunity in patients with non-small cell lung cancer (NSCLC) and malignant mesothelioma (MM).
Expand descriptionThis study looks at the effectiveness of the chemotherapy drug cyclophosphamide in combination with pemetrexed-based chemotherapy in people with advanced malignant mesothelioma or advanced non-small cell lung cancer receiving first or second line palliative treatment. Participants will all receive low-dose repeat treatment with cyclophosphamide in combination with the conventional dose of pemetrexed-based chemotherapy commencing from the second cycle of chemotherapy, up to a maximum of 6 cycles. Patients will be monitored for safety at the beginning of treatment, weekly whilst on treatment, and at 90-days follow-up. The tumour will be assessed on CT scan at baseline, after every 2 cycles of treatment, and at least 3 monthly after the completion of treatment, until any progression of the disease. The study aims to see whether this treatment is effective by improving the way the immune system reacts against the cancer by assessing the number/activation/proliferation of various immune cells from weekly blood tests taken at baseline, weekly whilst on chemotherapy, and at 90-day follow-up visit.
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Azithromycin in older people with airway disease
Expand descriptionThe primary purpose of the study is to further the identification of effective treatment options for people with obstructive airway diseases, such as asthma and chronic obstructive pulmonary disease, and neutrophilic inflammation. The study will investigate the anti-inflammatory effect of a macrolide antibiotic, azithromycin, on airway inflammation, symptoms, quality of life and lung function. It is hypothesised that azithromycin therapy will reduce bacteria in the sputum and inflammatory cells of participants with neutrophilic airway disease.
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A pseudo-randomised dietary intervention to evaluate the effects of a high protein diet on weight loss, body composition and other health outcomes in obese individuals who have gastric banding surgery.
Expand descriptionThis study aims to investigate the usefulness of a high protein diet for obese individuals who have undergone gastric banding. It is a pseudo-randomised control trial comparing a high protein diet with usual dietetic care after surgery. The intervention period will be of six months duration with a further six months of follow-up. This study will help to inform best practice nutritional management for individuals who have had gastric banding.
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Randomized trial of homocysteine lowering treatment of depression in later life (B-VITAge)
Expand descriptionOlder people with depression have higher plasma concentration of a chemical called homocysteine than non-depressed older adults. The use of some vitamins of the B group are effective in reducing the plasma concentration of homocysteine. We designed this trial to determine if the use of adjunctive treatment with B-vitamins improves the efficacy of antidepressant treatment for people aged 60 years or over.
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Predicting Adverse Pregnancy Outcomes (PAPO) Study: An observational study to determine factors in both male and female partners to predict healthy pregnancies and adverse pregnancy outcomes
Expand descriptionInvestigating possible causes or predictors of adverse pregnacy outcomes.
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A Multicenter, Open-Label Phase 1b/2 Study to Assess the Safety and Clinical Activity of Intravenous Combretastatin A1 Diphosphate (OXi4503, CA1P) as Monotherapy in Subjects with Primary or Secondary Hepatic Tumour Burden
Expand descriptionto Assess the Safety and Clinical Activity of Intravenous Combretastatin A1 Diphosphate (OXi4503, CA1P)