ANZCTR search results

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

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31201 results sorted by trial registration date.
  • Atrial Myopathy and Embolic Stroke (AMES) trial – Prospective Randomised Open Blinded Endpoint (PROBE) clinical trial with parallel cohort study

    This clinical trial will look at patients who have had an acute ischaemic stroke caused by a blood clot, but where doctors can't find a clear reason for it (this is called Embolic Stroke of Uncertain Source, or ESUS). The study will test whether a type of medication called DOAC (a stronger blood thinner) can help prevent future strokes and improve recovery in patients with atrial myopathy, a condition identified through ultrasound showing reduced heart chamber strain. Additionally, there will be a parallel study to confirm current and new tests for atrial myopathy that can help predict the chances of having another stroke.

  • Safety and feasibility of Intramuscular Dexmedetomidine for Delirium

    This is a pilot feasibility randomized clinical trial comparing the novel intramuscular use of dexmedetomidine, an alpha-2 agonist agent, in preventing delirium and improving sleep in older, non-ventilated intensive care patients, compared with usual care. The main aims are to determine if using the drug in this context is safe, and if further, larger studies would be feasible.

  • The feasibility and preliminary effectiveness of a machine learning (ML)-based digital assistant to promote physical activity in older adults

    The study aims to evaluate the feasibility and preliminary effectiveness of a machine learning (ML)-based physical activity digital assistant to promote physical activity in older adults 65 years of age or older. The study will use an existing ML-based digital assistant MoveMentor that applies natural language and reinforced learning in an engaging, interactive, and personalised intervention. This study will assess the feasibility (usability, acceptability, and engagement), preliminary effectiveness, and user experience. A feasibility study with non-randomised pre-post measures will be conducted over 14-weeks. At baseline (week 0) participants average step count will be tracked through an activity tracker, then complete a brief online survey to assess participant demographics, self-reported physical activity, and intentions to engage in physical activity. At the end of the intervention (week 13) participants will complete a further online survey to measure changes in self-reported physical activity, intentions to engage in physical activity, and user experience assessed through usability, acceptance and engagement with MoveMentor. The primary outcome is the change in steps recorded from baseline to post-intervention.

  • Examining the effectiveness of Breathwork on increasing resilience and psychological well- being while preventing and attenuating anxiety, depression, insomnia, and stress in emergency responders

    The study is a randomised controlled trial investigating the effect of breathwork on mental health outcomes in student paramedics. It involves two groups, with participants randomised to either the breathwork intervention or a control group, over a three-month period. The primary focus is to assess improvements in mental health metrics such as stress, anxiety, depression, insomnia, resilience and overall well-being. We hypothesise that the breathwork group will experience positive improvements in mental health, resilience and well-being, compared to the control group.

  • Investigating the impact of external factors on diurnal changes to corneal immune cells

    This study is investigating whether ‘time of day’ factors and sleep patterns affect immune cells (cells that protect the eye) in the cornea (transparent front part of the eye). This study will also examine whether different light filtering lenses (that block different wavelengths of light) influence the behaviour of corneal immune cells. The study will aim to enrol 24 participants, with a target of 18 completed participants, aged 18 to 45 years, who have healthy eyes and do not regularly wear contact lenses or spectacles for daily activities. Participants will attend for 8 study visits in total, comprising 3 visits in the morning (08:00 AM-10:00 AM) and 5 visits in the late afternoon (16:00 PM-18:00 PM). Over the course of the study, participants will be asked to wear various forms of eye wear, consisting of an eyepatch and safety glasses with a filtered lens over one eye, overnight and/or throughout the day, as directed by the study team, as well as have some tear and blood samples collected.

  • GRIP (Group Run Virtual Physiotherapy): A pilot study examining the feasibility of providing a physiotherapy-led falls prevention group exercise class via telehealth

    The study will look at the acceptability and suitability of older adults participating in an online group exercise class aimed at reducing the risk of falls. It will explore barriers and faciliators to a virtual falls prevention program. Participants included in the study will be recruited from RPA Virtual Hospital who meet a specific eligibility criteria. They will partake in a 12-week virtual falls prevention service that includes assessment and delivery of exercise. We are hoping that older adults will find the 12 week virtual falls prevention service acceptable and suitable for their needs.

  • TRI-ME: Trimetazidine to treat Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A double-blind, randomised, placebo-controlled efficacy trial

    Existing treatments for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are inadequate and ME/CFS therapy represents an unmet need of healthcare. Our aim is to assess the efficacy of trimetazidine, a metabolic agent, in treating ME/CFS in a double-blind, randomised, placebo-controlled clinical trial. Mitochondrial dysfunction has long been associated with inflammation and oxidative stress of ME/CFS and may be the potential final common pathway in the pathophysiology of ME/CFS. Trimetazidine increases metabolic efficiency in the mitochondria by promoting glucose oxidation rather than fatty acid oxidation (i.e. increased energy generation) and has anti-inflammatory and antioxidant properties. Importantly, in preclinical rodent studies confirmed trimetazidine increases mitochondrial function in the brain and facilitates longer swimming in the forced swim test without causing hyperactivity in the large open field. Trimetazidine was also identified using an atheoretical drug screening approach that showed trimetazidine to redress mitochondrial dysfunction. The therapeutic potential of trimetazidine is clear, Trimetazidine is highly accessible, affordable, and has regulatory approval to treat angina in Asia and Europe, making it particularly suitable to repurpose for ME/CFS.

  • Optimization of indocyanine green use in gall bladder removal surgeries

    Indocyanine green has been used in laparoscopic cholecystectomies for several years now to improve the visualization of patients’ extrahepatic biliary anatomy. Various doses and timings of indocyanine green have been used to improve visualization while reducing liver hyper fluorescence, with no optimization of either. The purpose of this study is to find an optimal dose and time to administer indocyanine green in laparoscopic cholecystectomies which are currently mostly conducted as day cases at St. Vincent’s Hospital in Melbourne, Australia. The primary hypothesis is that a lower dose of ICG administered within an hour of surgery provides better visualization of the extrahepatic biliary anatomy compared to the commonly-used higher dose.

  • The impact of emergency medicine pharmacists on medication safety for critically ill patients in the resuscitation area of an emergency department

    Medication errors are an important cause of harm in Emergency Departments (EDs). The resuscitation area of Emergency Departments are busy, high risk environments in which patients who are in a critical condition are treated. Pharmacists have demonstrated an ability to improve medication safety in EDs and improve medicine use. However, the resuscitation area does not usually have a dedicated pharmacist. The aim of this study is to determine if the presence of an ED pharmacist in the resuscitation area to assist with the treatment of very unwell patients has a benefit to these patients. The hypothesis for this study is that an emergency medicine Pharmacist in the ED resuscitation team setting will reduce medication errors, help doctors and nurses give critical medicines more quickly, improve documentation of medications on medication charts, and optimise patient outcomes.

  • Understanding the impacts of nutritional education to help in the treatment of age-related muscle loss

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