ANZCTR search results

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

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31433 results sorted by trial registration date.
  • The Effect of Head Posture on Collapsibility of the Human Upper Airway During Sleep, Sedation & Anaesthesia

    The aim of the study is to determine the effect of head posture on the collapsibility of the airway during aesthesia and sleep in subjects with and without obstructive sleep apnoea. It is hypothesized that the airway will be more collapsible in the flexed (chin tucked) position than in the neutral or extended position during sleep and anaesthesia.

  • The effect of fish oil on platelet function

    The purpose of this research is to examine how different fish oil (omega-3 fatty acids) concentrates can influence platelet activity and improve platelet function in males and females. There is evidence in the published literature that response to fish oil supplementation is influenced by a gender-specific manner. Moreover, fish oil supplements contain different concentration ratios of the active ingredients, EPA and DHA. This research project will determine how gender influences fish oil supplementation so that males and females can receive maximum benefit against cardiovascular disease risk.

  • Prospective clinical trial assessing the Nanos short stem femoral prosthesis in patients undergoing total hip replacement surgery

    We propose to undertake a prospective clinical trial assessing qualities of the short stem cementless femoral prosthesis Nanos by Smith & Nephew Pty Ltd. We will undertake a 10 year follow up, which will consist of bone mineral density (“DEXA”) scanning, Roentgenstereometric Analysis (“RSA”), conventional radiographs and functional assessment. Functional analysis will be undertaken by using EuroQuol Group 5-Dimension Self-Report Questionnaire (“EQ5D”) and the Oxford hip score (“OHS”). Follow up time points will include the preoperative visit, the inpatient stay, 6 weeks, 3 months, 12 months and 2 years, 5 years and 10 years post surgery reviews.

  • Fish Oil and Multivitamin Study in Healthy Adults.

    In Australia, the population is ageing due to lower birth rates and increased life expectancy. The implication of this changing demographic means that the age group with the greatest needs will be the elderly. Research in this area includes studies assessing the efficacy of fish oils and multivitamins to improve memory and cognitive function in the elderly. Research is also focussing on the potential neuroprotective effects of these supplements to protect the elderly from more insidious cognitive decline, such as Alzeimer’s disease. The primary aim of the current study is to investigate whether supplementing diets with fish oils and multivitmains improve cognitive function in a healthy cohort of women and men aged 50 to 70 years of age. This research could potentially have significant bearing on the cognitive health of the elderly as well as the predicted economic burden in decades to come. Based on previous research, it is hypothesised that diets supplemented with a high dose of fish oil will improve cogntive performance namely spatial working memory performance and attentional processes. It is also anticipated that a high dose of fish oil compliemented with a multivitamin will provide additional benefits to cognitive performance as the multivitamins will limit oxidation of the Omega-3's once they have been ingested.

  • Randomized clinical trial investigating effects of a multi-nutrient combination on mood, stress, sleep and cognition in healthy young adults

    Participants attend Swinburne University Hawthorn for one practice visit where they go through the screening questions and provide informed consent. They also practice all cognitive and mood tasks that they will be doing on their subsequent testing sessions. They are then randomised to receive either the multivitamin treatment or placebo for 4 months. Participants come in for 3 testing sessions, the first one week later (V1), the second 2 months later (V2) and the third and final visit after 4 months (V3). At each testing session they complete congitive and mood assessments, together with blood flow, arterial stiffness, saliva cortisol, sleep quality and blood biomarker assessments. A subset of participants (40 males and 40 females) will also complete weekly cognitive and mood tests from home using mobile phones provided. Another subset of participants (40 males and 40 females) will also complete Steady State Probe Topography (SST) brainwave recording at Baseline, V2 and V3.

  • A phase 2, twelve month, randomized, controlled trial of combined treatment for exudative age related macular degeneration with variable dosing Ranibizumab (Lucentis) and Sub-Tenon Triamcinolone (Kenacort-A 40).

  • Efficacy of the Take a Breath Parent Program: A Randomised Controlled Trial for parents of children with a serious childhood illness/injury.

    This project will evaluate the efficacy of the Take a Breath Parent Program, which targets parents from three months following a traumatic event (their child's diagnosis of a serious childhood illness/injury). The overall aim is to assess if the Take a Breath Parent program leads to improvements in psychosocial distress for parents exhibiting early signs of posttraumatic stress. Specifically the trial will assess if participation results in: improvements in parental psychological flexibility, committed actions, valued living and quality of life and reductions in parental posttraumatic stress symptoms, experience of the illness/injury as distressing, and referrals to additional supports (e.g., mental health/counselling). Secondly improvements in child quality of life and child behaviour, family functioning and postive outcomes of the illness/injury will be assessed.

  • Popping the bubble wrap- unleashing the power of play: an innovative playground intervention to increase children's physical activity

    Disturbing numbers of children in Australia are overweight, bullied or have poor mental health – problems that are often inter-related. Recent decreases in outdoor play may be partly responsible. Outdoor play “pulls for” social interaction and physical activity; indoor play is often sedentary and solitary. Most young children love active outdoor play but parents and teachers fear injury. This project is a school-based intervention to increase outdoor play by: (1) adding 'loose part' materials to the playground and (2) helping adults change their views of risk associated with active play. We expect to demonstrate a significant effect on children’s activity levels, coping and social skills through strategies that are replicable in every school playground in the nation and to contribute to policy regarding play, health, and education.

  • Development of a Peer-support based Cardiac-Diabetes Self-Management Program: A study protocol

    People with cardiac disease who have type 2 diabetes have higher readmission rates (22%) than those without diabetes (6%) (Wu & Chang, 2008). Although self-management is an effective approach to achieve better health outcomes, there are no such programs specifically designed for patients with both conditions. Such programs need to be enhanced by user-friendly technology and supported by patient peers. This project aims to extend the development of a peer support based Cardiac-Diabetes Self-Management Program (CDSMP) by preparing a DVD to support persons' engagement in follow-up study.

  • Study of Lenalidomide Maintenance Versus Placebo in Responding Elderly Patients With Diffuse Large B cell Lymphoma (DLBCL) and Treated With Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP)

    In patients between 60-80 years with diffuse large B cell lymphoma (DLBCL), the current standard treatment is R-CHOP chemotherapy (consisting of the drugs Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone). However the probability of being alive and free of lymphoma 5 years after diagnosis is only 54%. Lenalidomide is an immune system modulating drug that has anti-lymphoma properties demonstrated in smaller studies of patients with relapsed/refractory DLBCL. Given the high risk of relapsed DLBCL in this older patient population this study is aimed at determining whether Lenalidomide maintenance taken orally for 21 days every 4 weeks can safely reduce the risk of progression/relapse of DLBCL. Who is it for? This study is open to patients aged between 60 and 80 years and currently underoing R-CHOP combination therapy for diffuse large B-cell lymphoma. Trial details Participants will be randomised into one of two arms, (1) 25mg daily lenalidomide for 21 days of a 28 day cycle of maintenenace therapy for up to 26 cycles, or (2) a placebo instead of the active drug over the same period. The aim of the study is to reduce the risk of progression/relapse of DLBCL

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