ANZCTR search results

These search results are from the Australian New Zealand Clinical Trials Registry (ANZCTR).

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32898 results sorted by trial registration date.
  • Azithromycin bronchiolitis Intervention Study 2: An multicenter intervention study for bronchiolitis in Darwin Townsville and Auckalnd - Comparing severity of disease and readmission of infants given azithromycin or placebo.

    In a previous study on bronchiolitis in Aboriginal children we found that 67% were from remote communties and required retrievals. A recent study has also shown that almost 2.5% of Aboriginal children in Australia's Northern Territory will be hospitalised for bronchiolitis more than once before reaching the age of 18 months. Multiple hospitalised respiratory infections and the severity of these infections are risk factors for developing chronic lung diseases including bronchiectisis and asthma. It is planned that this study will provide an estimation of the effect of azithromycin on the severity of bronchiolitis in Aboriginal and non Aboriginal infants. Assessing redmission for respiratory illness within 6 months may provide some indication of the medium term benefit of three doses of azithromycin, given to infants in the acute phase of viral bronchiolitis, in reducing the risk of further respiratory illness requiring hospitalisation.

  • A longitudinal study of caries development in children from 4 to 15 years of age

    In this study we will continue to follow participants recruited to " A longitudinal study of caries prevention in children aged two to four years" HREC/09/QPAH/158, ACTRN12609000330246 who have undergone preventative methods of education, home visits and toothbrushing with fluoride toothpaste, 0.12% chlorhexideine gel and CPP-ACP Tooth Mousse. The effectiveness of these strategies will be assessed through -microbial analysis for the presence of decay causing bacteria - clinical dental examination data - statistical analysis of data for case and control groups

  • Intrathecal baclofen therapy for management of spasticity: An Australian paediatric multicentre prospective audit.

    Intrathecal baclofen (ITB) therapy is used to manage severe spasticity. ITB therapy is available to children and adolescents at 6 tertiary Paediatric hospitals in Australia. ITB is a new therapy, with 12-15 ITB pumps implanted in Australian children and adolescents each year. There is no standard pre assessment tool or follow up protocol for children and adolescents receiving ITB therapy in Australia. The objective of this study is to identify and collect a minimum data set for assessment and follow up of children and adolescents receiving ITB therapy in Australia. Two of the aims of this study are (1) Identifying which assessment tools are useful at assessing the effect of ITB upon your child’s daily functioning; and, (2) document the complications associated with ITB therapy. For the purposes of data collection a prospective multicentre audit is proposed. This would include children attending Princess Margaret Hospital for Children (Perth), Royal Childrens Hospital (Melbourne), Monash Medical Centre (Melbourne), Westmead Childrens Hospital (Sydney), Women & Childrens Hospital (Adelaide) and the Royal Childrens Hospital (Brisbane). All Australian children and adolescents who are offered ITB therapy will be asked to enrol in this audit. A standardised assessment protocol will be utilised by each centre to capture data across each domain of the World Health Organsiation international classification of functioning, disability and health. Participation in this prospective audit reflects standard care and is voluntary.

  • The role of vitamin D in the treatment of nerve pain in diabetes

    Vitamin D deficiency is common amongst people with type 2 diabetes. People with type 2 diabetes frequently develop painful neuropathy ("nerve pain" especially in the feet). The study hypothesis is that vitamin D supplementation may improve symptoms of nerve pain. The study is therefore designed to investigate the impact of vitamin D supplementation on nerve pain in people with type 2 diabetes

  • Removal Of Cyclosporine With Everolimus On Inflammation And Vascular Endpoints

    The purpose of this study is to determine the safe and potential cardiac (heart) benefit of using Certican (Registered Trademark) in kidney transplantat patients in combination with Neoral (Registered Trademark) (cyclosporine A), corticosteroids (methylprednisone/prednisone) and myfortic (Registered Trademark) (mycophenolate) with or without Simulect (Registered Trademark). The main goal is to reduce the risk of heart disease. Certican (Registered Trademark), Neoral (Registered Trademark), Simulect (Registered Trademark), corticosteroids and myfortic (Registered Trademark) are all anti-rejection treatments.

  • Paediatric Influenza Vaccine Outcome Trial (PIVOT)

    Influenza is a viral illness that causes much social disruption. It causes serious complications in young children including hospitalisation. Children in child care settings are more likely to be infected. Influenza vaccination can help prevent influenza in adults but data are lacking in young children. This study will determine both direct child benefits (protection, continuity of day care) and indirect benefits of influenza vaccination in reduced work absence (staff, parents), illness in the extended family. The study also measures the social and economic impact of influenza vaccination.

  • A randomised controlled trial of vitamin D supplementation vs placebo on cognitive and emotional outcomes

    There is a growing body of research indicating that vitamin D blood concentrations can impact on brain functioning. In particular, there is robust evidence in animal models showing that vitamin D deficiency during development impairs brain functioning in adulthood. However, no studies have examined whether enhancing vitamin D blood concentrations by vitamin D supplementation during adulthood can improve brain functioning. This study will assess whether increasing vitamin D blood concentrations via vitamin D supplementation in healthy adults improves various aspects of brain functioning such as attention, response inhibition, and general mood and emotions. We anticipate that this study will provide us with important information about the effects of enhancing vitamin D blood concentrations on brain function in healthy adults.

  • Evaluation of the effects of increasing amounts of protein in test meal on gastrointestinal hormone secretion, appetite and energy intake in lean and overweight subjects

    There are a number of dietary approaches, including restriction of total energy or fat, or increasing dietary protein and reducing carbohydrate to try and induce weight loss. Protein is commonly believed to be the most satiating macronutrient, however no studies have investigated the effects of protein in an oral preload on satiety and energy intake, taking into consideration the daily energy requirements of individual subjects. Therefore the purpose of the study is to compare the effects of high-fat, high-carbohydrate and high-protein oral preloads and the effects of increasing amounts of protein in an oral preload on gastrointestinal hormone secretion, appetite and energy intake in lean and overweight subjects.

  • An evaluation of platelet activation and function in different haematological disorders pre and post treatment using flow cytometry and extracellular regulatory kinase pathway

    Although most patients with different haematological disorders present with either bleeding or clotting, there is little known about how patients develop these complications and what risk factors are involved. Platelets are an essential component of haemostais to stop bleeding and also in case of their activation may give rise to thrombosis. So it is important to study the role of platelet-function and activation in the patients who are diagnosed with different haematological disorders/cancers and receiving treatment. Studying platelets function and activation with various new techniques will give us a better understanding of platelets activity in haematological malignancies such as leukaemia, lymphoma, myeloma or other haematological disorders who present to the Launceston General Hospital (LGH), Tasmania, Australia. With the help of the Flow Cytometer and also as a part of PhD degree at University of Tasmania (UTAS), School of Human Life Sciences, we are aiming to establish different methods of studying platelets activation and function in different haematological malignancies in order to examine the theory of these malignancies and rheir association with platelet activation and or dysfunction. Significance of the Project: The availability of fluorescent monoclonal antibodies and probes provides a powerful tool for the investigation of platelet function by flow cytometry. To date, most platelet function analysis by flow cytometry has focused on the involvement of platelets in thrombotic disorders and acute coronary syndromes. One area where research has been limited is in oncology patients, including those with malignant e.g. leukaemia, lymphoma, multiple myeloma, and benign e.g. immuno thrombocytopenia and thrombocytopenic purpura, haematological disorders, where patients usually present with either bleeding or thrombosis symptoms. It is well documented that bleeding is quite common in these patients often leading to more intensive platelet intervention and sometimes poorer prognosis. Thrombocytopenia is usually evident due to the late diagnosis of disease with subsequent marrow replacement or as a consequence of the treatment. However, the effect of platelet dysfunction may also contribute more significantly than is currently known. Patients with haematological disorders who bleed often receive platelet transfusions. Although this approach usually rectifies the bleeding to suggest the defect is quantitative, it is not known whether abnormal platelet function also contributes to the bleeding diathesis in these patients. Indeed, this is yet to be corroborated given that donor platelets are initially healthy and unaffected when transfused so offer both volume and functionality to the patient before disease or drug regimens have any affect on them.

  • A Double Blind Placebo Controlled Randomised Trial of PF-804 in Patients with Incurable Stage IIIB / IV Non-small Cell Lung Cancer After Failure of Standard Therapy for Advanced or Metastatic Disease

    This study looks at the effectiveness of treatment with the drug PF-804 in patients with incurable non-small cell lung cancer, where standard therapy for advanced or widespread disease has not been successful. Who is it for? You can join this study if you have a confirmed diagnosis of non-small cell carcinoma of the lung, described as incurable stage IIIB or IV, where standard therapy has not been successful. Trial details Participants will be randomly divided into two groups. One group will receive a non-active (placebo) treatment, and the other will receive treatment with the drug PF-804, both taken orally (in cycles of 28 days)until the disease progresses or toxicity is unacceptable. The aim is to compare the overall survival between the two groups, and to monitor the effects of the treatment. PF-804 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

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