ANZCTR search results

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

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32712 results sorted by trial registration date.
  • A study to compare the effect of three burns dressings on burns in children

    At the Royal Children's Hospital in Brisbane the standard of care in burns dressings for small to medium partial thickness burns has changed over the years. Currently, silver containing dressings are used to prevent infection and promote healing. However despite the large number of burns dressings available on the market, very few high level trials have been conducted in children or adults. This study aims to determine the effect of various silver and silicone containing burns dressings for the treatment of partial thickness burns in children. The study hypothesises that: 1. Rate of healing, need for grafting and subsequent scarring from a burn wound is partly determined by the choice of dressing used. 2. The choice of dressings used can partly assist with pain and anxiety strategies during dressing change procedures; and impacts on a child's comfort and engagement in activities. 3. The dressing which best fulfils the above qualities will also be the most cost effective.

  • Pilot of a self-help app to support suicide prevention amongst Indigenous youth

    This project aims to investigate whether a self-help interactive program delivered via tablet devices can help Indigenous youth to reduce their suicidal ideation. Participants will be randomly assigned to either the intervention group, which includes therapeutic activities grounded in acceptance and commitment therapy or a wait list control group. We predict those using the intervention program will report reduced suicidal ideation and mental distress after using the program for 6 weeks.

  • Studying an online educational course for supporting emotional health of dialysis patients

    This study is to evaluate the feasibility, effectiveness, and acceptability of an internet-delivered treatment program for depression and anxiety amongst dialysis patients using an open trial design (pilot study). The study also aims at modifying the content and materials to enhance the treatment acceptability and effectiveness by obtaining participants’ feedback and incorporating the evidence-based components specific to dialysis patients

  • Surgery for the treatment of Otitis Media in Indigenous children, surgical sub-study

    Otitis media (OME/AOM) is a major problem amongst Indigenous children living in remote Australian communities. Medical treatment often fails and ENT surgeons are called upon to provide surgical care. This multi-centre randomised trial compares the outcomes of two current treatments (Myringotomy/ adenoidectomy V grommet tubes/ adenoidectomy). There are 11 sites proposed across WA, NT & N Qld. 280 Indigenous children aged 3-10 years will be randomized into 2 groups; (1) adenoidectomy with ventilation tubes (VTA) (2) adenoidectomy with myringotomy only (MA) The children will be followed up with monthly phone calls for 12 months following surgery by which time the OM will likely have recurred if were to do so. At the end of 12 months study staff will visit the children in their community for hearing assessments and nasal swabs. The outcome measures will be a reduction in the prevalence of OME/AOM, hearing impairment, aural discharge / perforation, and the also effect of treatment on nasal colonisation with pathogenic bacteria.

  • A Research Study of Injections of Testosterone in an Oil Vehicle for men with Androgen Deficiency: Reandron (Testosterone Undecanoate) will be administered subcutaneously and intramuscularly.

    Although intramuscular (IM) injections of androgen's are known to be effective, they result in varying degrees of pain at the injection site that may last for a day or two. These injections need to be given into a precise location of the buttocks and require staff with expert training. Unlike many other injections these cannot be self-injected due to the difficulty of safely injecting into the buttocks. A SC injection, if effective, may be given by yourself in your own home, which would be more convenient to avoid extra medical visits as well as saving GP and hospital resources. Many men who require androgen replacement therapy may have bleeding disorders or are on medications that may intentionally slow the ability of their blood to clot. These men have a theoretical risk of bleeding and a very large bruise deep in an important muscle may later become infected and cause significant disability. As a result men using these anti-clotting drugs are usually prescribed other forms of androgen replacement therapy that are not always optimal. A subcutaneous (SC) injection, if effective, may be used in these men. This is a randomised crossover study of testosterone Undecanoate given subcutaneously and intramuscularly in patients receiving testosterone replacement therapy. Each participant will receive a single IM injection and a single (SC) injection of TU. An IM injection is standard of care and duration of action is approximately 12 weeks. It is expected a SC injection will have a duration of action of 12 weeks. Thus the study will take 24 weeks for each participant to complete both arms. This is the second stage of a 2 stage research study. This is stage 2 of study ACTRN12613000068763

  • Combination of Selenium and Green Tea on bowel health

    This study will evaluate whether combination dietary supplementation of selenium and green tea can reduce the risk of developing bowel cancer in healthy humans. Who is it for? You may be eligible to join this study if you are a healthy man or woman aged between 50-75 years, with no active bowel disease. You should have no previous colorectal cancer and no allergy or intolerance to nuts or green tea products. Trial details Participants will be randomly (by chance) divided into three groups. Participants in one group will eat 6 brazil nuts per day (providing 48mcg selenium/day). Participants in the second group will take 4 green tea extract capsules daily. A third group will take both of these in combination. All dietary interventions are continued for 6 weeks. Participants will be required to give blood samples and rectal biopsies before and after treatment (at 6 weeks) in order to assess response to the different dietary interventions. This study will provide valuable information on how a combinational dietary approach may reduce the risk of developing colorectal (bowel) cancer in humans.

  • A study on the effectiveness of Indomethacin in preventing post Endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis

    We propose a randomised control study to assess the use of prophylactic Non-steroidal Anti-inflammatory Drugs for the prevention of Post Endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis.

  • The Effect of Goal Directed Fluid Therapy using an Oesophageal Doppler in Renal Transplant Surgery

    Accurate fluid management in the peritransplant period is crucial. In many cases the donor renal allograft will have established acute tubular necrosis due to prolonged cold ischaemic time and will therefore have delayed graft function. A common complication of transplant surgery is over aggressive fluid replacement in a patient who is essentially anuric which may precipitate pulmonary oedema requiring urgent dialysis. On the other hand, inadequate volume replacement in a renal allograft recipient who has immediate graft function can result in hypovolaemia and potentially delayed graft function. The ODM has been used in case series of renal transplantation demonstrating efficacy and safety. This prospective, randomized trial looks at goal directed fluid therapy using the oesophageal doppler monitor versus standard of care fluid therapy in renal transplant patients to determine if there is a reduced length of stay and reduced incidence of delayed graft function.

  • Sports-related concussion and its correlates among current and retired professional rugby league players

  • A comparison of humidified and unconditioned gases in the delivery room for stabilising preterm infants less than 30 weeks gestation at birth

    Infants born very prematurely (under 30 weeks gestation) often require support with their breathing after birth as their lungs are stiff and they find it hard to fill them with air. In order to help infants breathe we use a flow of gas (oxygen and air) to provide pressure to help open their lungs. In this study we are comparing whether it is better to use a gas flow that has been warmed and moistened (humidified), compared to the standard method of using gas directly from the cylinder or wall (unconditioned). Humidifying gases is routine within the setting of the neonatal intensive care but is not extended to use in the delivery room setting. The purpose of this study is to find out whether the use of humidified gases in the delivery room is better in helping premature infants stay warm immediately after birth. The primary outcome will be measurement of rectal temperature on admission to the neonatal and intensive care unit (NISC).

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