ANZCTR search results

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

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31615 results sorted by trial registration date.
  • Epoetin and cardiac function:An echocardiographic analysis in patients with heart failure.

    A preliminary study to evaluate the acute effect (2 hours) of a commonly used treatment for anaemia in renal failure on cardiac function (strength) in patients with cardiac failure.The potential benefits are based on a recent study(unpublished) that observed an effect of intravenous epoetin alpha on heart and large blood vessel (aorta) function.Patient and echocardiographer blinded to treatment/placebo order.

  • Efficacy study of adding chemotherapy to radiotherapy for treating bladder cancer

    Radiation and chemotherapy both work in people with muscle-invasive bladder cancer. This study will determine if giving them together improves the results for people with this disease that seems to be confined to the bladder, but who are felt to be suitable candidates for bladder preserving treatment.

  • A randomised clinical trial (RCT) of the effect of Neuro-Emotional Technique (NET) on the clinical manifestations of primary overt hypothyroidism

    This project is a comparative study investigating the effects of Neuro-Emotional Technique (NET) treatment on Hypothyroidism. Hypothyroidism is defined as any condition that results in a decrease in the amount of circulating thyroid hormones in the body. NET is a therapeutic procedure developed by Chiropractors as an adjunct to standard Chiropractic techniques. The development and structure of this technique ties in with the biopsychosocial model of health care, which represents a holistic approach to patient management. General aims: -To determine the effect of Neuro-Emotional Technique (NET) in the treatment and management of primary hypothyroidism. Specific Aims: - To determine the emotional/ psychological/ social/ hormonal profile of a group of primary overt hypothyroid participants. - To determine if the emotional/psychological/ social/hormonal profile of a group of primary overt hypothyroid participants changes with NET treatment. - To determine if primary overt hypothyroidism can be affected by NET treatment in the short term (2 months) and the medium term (6 months) Interpretation of Results and Discussion Accumulated data will be statistically analysed using T-tests, longitudinal analysis with an alpha value of 0.05

  • Novel treatments for alcohol dependence: A randomized controlled trial of structured stepped-care intervention for psychiatric comorbidity

    Co-morbid depression and anxiety are becoming a critical issue in the management of alcohol dependence due to the high prevalence, debilitating effects and lack of effective treatment options. This proposal seeks to generate and evaluate a novel, integrated treatment for comorbid anxiety or depressive disorder. Participants will all receive anti-craving medication (naltrexone and/or acamprosate) and formal assessment of clinically relevant anxiety or depression. They will then be randomized to receive either a usual counselling care or a CBT ‘stepped-care’ intervention including a manual-based psychotherapy appropriate for their psychiatric profile. Participants will be followed up at 3 and 6 months to determine the benefits of integrated treatment on alcohol consumption, comorbid symptoms and health. It is hypothesised that stepped care for alcohol dependence with comorbid mood or anxiety disorders will result in less relapse and lower alcohol consumption compared to usual care, and result in a greater improvement in comorbid symptoms and quality of life compared to usual care.

  • HABITS Hormonal replacement therapy after breast cancer diagnosis - is it safe?

    Menopausal symptoms are common in women treated for early breast cancer. Hormone replacement therapy (HRT) is very effective at relieving menopausal symptoms, but we do not know if HRT is helpful or harmful for women who have had breast cancer. This trial will determine the effects of HRT in women who have been treated for early breast cancer. The trial aims to include 1300 women from around the world who will be treated with either HRT or the best non-hormonal alternative treatment while being closely monitored by their cancer specialists and gynaecologist.

  • IBCSG VIII - Adjuvant therapy in pre- and peri-menopausal patients with node negative breast cancer

    IBCSG VIII is a randomised clinical trial designed to test the therapeutic role of short duration ovarian function suppression (using Zoladex) in pre-/perimenopausal patients with node negative breast cancer.

  • The Effect of an Infant Sleep Behavioural Intervention to Treat Infant Sleep Problems on Infant Sleep and Maternal Mental and Physical Health: A Clustered Controlled Trial

    The study aims to determine whether a brief, primary-care behavioural intervention, designed to manage infant sleep problems, can improve both infant sleep and symptoms of maternal depression. Up to 45% of parents report a problem with their infant’s sleep in the second six months of life whilst up to 15% of Australian mothers are affected by postnatal depression. There is a strong link between infant sleep problems and postnatal depression. This intervention has the potential to reduce the twin burdens of both sleep problems and postnatal depression and therefore significantly improve the wellbeing of mothers, their children and their families.

  • IBCSG 13-93 - Adjuvant therapy for premenopausal patients with node positive breast cancer who are not suitable for endocrine therapy alone

    This clinical trial is for premenopausal women who after their breast cancer surgery are found to have breast cancer which is not suitable for hormonal treatment alone, and who also have cancer cells in the glands of the arm pit ('positive axillary lymph nodes’). It is known that these women will benefit substantially by having chemotherapy after surgery for breast cancer. The optimal chemotherapy program involves two short courses of different chemotherapy programmes (AC [doxorubicin or epirubicin + cyclophosphamide] & CMF [cyclophosphamide, methotrexate, 5-fluorouracil). It is not known whether the second chemotherapy course (CMF) should begin immediately after the first course (AC) or whether it should be delayed with a break in between. Whether or not a patient will have a gap between her chemotherapy programmes, as well as whether she will have Tamoxifen or not will be allocated by a process called randomisation which is similar to tossing a coin. This trial will test whether the delay between the chemotherapy courses is needed as well as if there is an extra benefit of adding a hormonal treatment to the chemotherapy.

  • IBCSG 14-93 - Adjuvant therapy for post/peri menopausal patients with node positive breast cancer who are not suitable for endocrine therapy alone

    This clinical trial is for post and perimenopausal women who after their breast cancer surgery are found to have breast cancer which does not contain hormone receptors (is not stimulated by hormones), and who also have cancer cells in the glands of the arm pit (‘positive axillary lymph nodes’). It is known that these women will benefit substantially by having chemotherapy after surgery as well as long term hormonal treatment for their breast cancer. The optimal chemotherapy program involves two short courses of different chemotherapy programmes (AC & CMF). It is not known whether the second chemotherapy course (CMF) should begin immediately after the first course (AC) or whether it should be delayed (with a break in between). Whether or not a patient will have a gap between her chemotherapy programmes will be allocated by a process called randomisation which is similar to tossing a coin. This clinical trial will assess which method of giving chemotherapy is optimal for decreasing the chance of breast cancer recurrence and increasing patient survival.

  • Intergroup Exemestane Study (IES)

    At present, it is standard for women with early breast cancer to receive five years of treatment with tamoxifen, following surgery. For many women, tamoxifen reduces the risk of breast cancer returning. However, some information suggests that tamoxifen may be of most benefit in the two to three years after surgery, after which it becomes less effective. The Adjuvant Exemestane trial will test whether it is better to take five years of tamoxifen, or to begin a new treatment (exemestane) after two to three years of tamoxifen, for the remainder of the five years. Exemestane is effective in patients with advanced cancer who have already been treated with tamoxifen and had their cancer return. Internationally, 4400 postmenopausal women who have had early breast cancer and taken two to three years of tamoxifen treatment will take part in the trial, and be given either exemestane or more tamoxifen to finish five years of treatment. It is hoped that switching treatments will be more effective at lowering the risk of breast cancer returning than continuing tamoxifen, and it may also lower the risk of developing long-term side effects from tamoxifen.

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