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data | trial_id |
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We will now compare two CS treatment regimens: short course (72 hours only) of high dose versus more conventional, moderate dose therapy over 14 days in terms of efficacy and adverse events (AE). At the same time, we will continue our work to delineate the aetiological factors and inflammatory processes underlying AECOPD.This project will test the following hypotheses:1 Systemic CS are effective during AECOPD because of a rapid reduction in neutrophil chemotactic cytokines and down-regulation of neutrophil-related vascular adhesion molecules; this occurs over the first 2-3 days of therapy.2. Thus, short-course, high-dose CS therapy is as efficacious in the treatment of AECOPD as a more conventional 14-day course of moderate dose CS, but with significantly less risk of AE and without rebound of inflammation after cessation. Hospital length of stay can be reduced.3.Exacerbations over the subsequent one month (treatment failure) are no more frequent with short versus conventional course CS therapy.4. Viral and bacterial organisms isolated from sputum during an AECOPD are associated with a greater inflammatory response within the airway than non-infective exacerbations, but both are responsive to CS therapy.Specific aims are:1.To build on our preliminary findings of a rapid reduction in sputum neutrophilia and improvement in symptoms by systemic CS during AECOPD and to examine whether this relates to inhibition of neutrophil-related chemotactic factors and vascular adhesion molecules. 2.To compare short-course (3 day), high dose CS treatment and more conventional 14-day moderate dose CS therapy with focus on clinical outcomes, reductions in airway inflammation, rebound exacerbation and adverse events. 3.To identify bacterial and viral organisms as well as determine bacterial load at admission and to then relate these to airway inflammation, response to treatment and rate of rebound.', ''), ('Trial_Details_Control_Update_Value_Step3_10', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_10', 'Reason:', '', 'hidden'), ('', 'Trial website:', '', ''), ('Trial_Details_Control_Update_Value_Step3_11', 'Update:', u'', 'hidden'), ('', 'Presentations / publication list:', '', ''), ('Trial_Details_Control_Update_Value_Step3_12', 'Update:', u'', 'hidden'), ('', 'Name:', 'Dr David Reid', ''), ('Trial_Details_Control_Update_Value_Step3_13', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_13', 'Reason:', '', 'hidden'), ('', 'Address:', 'Clinical School of Medicine\n43 Collins Street\nHobart TAS 7001', ''), ('Trial_Details_Control_Update_Value_Step3_14', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_14', 'Reason:', '', 'hidden'), ('', 'Country:', 'Australia', ''), ('Trial_Details_Control_Update_Value_Step3_15', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_15', 'Reason:', '', 'hidden'), ('', 'Tel:', '+61 3 62267043', ''), ('Trial_Details_Control_Update_Value_Step3_16', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_16', 'Reason:', '', 'hidden'), ('', 'Fax:', '+61 3 62264894', ''), ('Trial_Details_Control_Update_Value_Step3_17', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_17', 'Reason:', '', 'hidden'), ('', 'Email:', 'D.E.C.Reid@utas.edu.au', ''), ('Trial_Details_Control_Update_Value_Step3_18', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_18', 'Reason:', '', 'hidden'), ('', 'Name:', 'Dr Himanshu Garg', ''), ('Trial_Details_Control_Update_Value_Step3_19', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_19', 'Reason:', '', 'hidden'), ('', 'Address:', 'Clinical School of Medicine\n43 Collins Street\nHobart TAS 7001', ''), ('Trial_Details_Control_Update_Value_Step3_20', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_20', 'Reason:', '', 'hidden'), ('', 'Country:', 'Australia', ''), ('Trial_Details_Control_Update_Value_Step3_21', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_21', 'Reason:', '', 'hidden'), ('', 'Tel:', '+61 3 62264846', ''), ('Trial_Details_Control_Update_Value_Step3_22', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_22', 'Reason:', '', 'hidden'), ('', 'Fax:', '+61 3 62264894', ''), ('Trial_Details_Control_Update_Value_Step3_23', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_23', 'Reason:', '', 'hidden'), ('', 'Email:', 'hgarg@utas.edu.au', ''), ('Trial_Details_Control_Update_Value_Step3_24', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_24', 'Reason:', '', 'hidden'), ('', 'Name:', '', ''), ('Trial_Details_Control_Update_Value_Step3_25', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_25', 'Reason:', '', 'hidden'), ('', 'Address:', '', ''), ('Trial_Details_Control_Update_Value_Step3_26', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_26', 'Reason:', '', 'hidden'), ('', 'Country:', '', ''), ('Trial_Details_Control_Update_Value_Step3_27', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_27', 'Reason:', '', 'hidden'), ('', 'Tel:', '', ''), ('Trial_Details_Control_Update_Value_Step3_28', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_28', 'Reason:', '', 'hidden'), ('', 'Fax:', '', ''), ('Trial_Details_Control_Update_Value_Step3_29', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_29', 'Reason:', '', 'hidden'), ('', 'Email:', '', ''), ('Trial_Details_Control_Update_Value_Step3_30', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_30', 'Reason:', '', 'hidden'), ('', u'', u'', '')] | 14 |
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[] | 19 |
[] | 20 |
[] | 21 |
[] | 22 |
[] | 23 |
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Respir Med. 2008;102(5):738-43.3.\tWalters J, Johns DP, Blizzard L, Walters EH, Wood-Baker R. Effects of 4.\tfeedback on spirometry in primary care on motivation for smoking cessation. Journal of Smoking Cessation. 2009;4(1):34-41.5.\tWalters J, Wood-Baker R, Walls J, Johns D. Stability of the EasyOne ultrasonic spirometer for use in general practice. Respirology. 2006;11(3):306-10.6.\tWalters JA, Hansen E, Mudge P, Johns DP, Walters EH, Wood-Baker R. Barriers to the use of spirometry in general practice. 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u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_8', 'Reason:', '', 'hidden'), ('', 'Secondary sponsor:', u'None', ''), ('', 'Name:', u'Nil', ''), ('', 'Address:', u'', ''), ('', 'Country:', u'', ''), ('', 'Other collaborator:', u'', ''), ('', 'Has the study received approval from at least one ethics committee?', 'Yes', ''), ('Trial_Details_Control_Update_Value_Step3_9', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_9', 'Reason:', '', 'hidden'), ('', 'Ethics Committee name:', u'RCH Melbourne', ''), ('', 'Address:', u'', ''), ('', 'Country:', u'Australia', ''), ('', 'Date of approval:', u'', ''), ('', 'HREC Number:', u'', ''), ('', 'Countries of recruitment:', u'Australia', ''), ('', 'Brief summary:', 'The need for supplying fluids in paediatric bronchiolitis (severe viral airway infection of the infant) is frequent, and is the consequence of reduced feeding, sweating, and fever., There are currently 2 means of supplying fluids, intravenous or nasogastric.Nasogastric rehydration (NR) means giving fluids through a feeding tube inserted through the nostrils into the stomach thus eliminating the effort of drinking. It is generally effective and has few complications. Intra venous rehydration (IR) means giving fluids directly into a vein through a drip. It is often difficult to insert a drip in this particular age group, whereas the nasal feeding tube is generally easier to insert. The potential complications of IR are water overload and electrolyte imbalances. The main possible complications of NR is vomiting. The role of NR in bronchiolitis is, however, controversial. It is, for example, an accepted treatment in Scandinavia and Switzerland, whereas IR is the accepted treatment at the RCH Melbourne. Even within Australia there is no standard of care as such among the different hospitals with most hospitals using a combination of NR and IR, without any guidelines. The little existing evidence shows that NR in bronchiolitis is safe and well tolerated.The major concern raised with NR is the partial obstruction of the airway, by cousing ablockage of the nostril in young children who mostly breathe through the nose, thus theoretically causing further breathing problems. 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Patients with other medical or psychiatric problems, which in the opinion of the investigator preclude them from participating in the study.10. Patients unwilling to return for follow up visits.11. Patients participating in another experimental protocol.12. Patients who are pregnant or breast-feeding.13. Claustrophobia or orthopaedic difficulties that would impede nuclear scanning.14. Patients must be deemed haemodynamically stable:-Minimum systolic blood pressure of 90mm Hg -Urine output less than 0.5cc/kg/hr for a period of eighteen hours or greater would exclude patient from study -Patients cannot be using inotropic agents such as dopamine, dobutamine, levophed, adrenaline, noradrenaline, amrinone, or milrinone.15. Patients must not have signs, symptoms or biochemical evidence of multi-organ failure.16. 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[] | 63 |
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[('', '', '', ''), ('rowRequestNumber', 'Request Number:', '000079', ''), ('rowACTRNumber', 'ACTR Number:', 'ACTRN12605000080628', ''), ('rowStatus', 'Trial Status:', 'Registered', ''), ('rowSubmittedDate', 'Date Submitted:', '27/07/2005', ''), ('rowRegisterdDate', 'Date Registered:', '5/08/2005', ''), ('Trial_Details_Control_rowDateUpdated', 'Date Last Updated:', '11/03/2008', ''), ('Trial_Details_Control_rowTrialType', 'Registration Type:', 'Retrospective', ''), ('', 'Public title:', 'Passive joint mobilisation for the treatment of shoulder pain and stiffness', ''), ('Trial_Details_Control_Update_Value_Step1_1', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step1_1', 'Reason:', '', 'hidden'), ('', 'ANZCTR registration title:', 'The effect of passive joint mobiisation on shoulder pain and disability in the treatment of shoulder pain and stiffness', ''), ('Trial_Details_Control_Update_Value_Step1_2', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step1_2', 'Reason:', '', 'hidden'), ('', 'Secondary ID:', u'', ''), ('', 'UTN:', '', ''), ('Trial_Details_Control_Update_Value_Step1_15', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step1_15', 'Reason:', '', 'hidden'), ('', 'Trial acronym:', '', ''), ('Trial_Details_Control_Update_Value_Step1_3', 'Update:', u'', 'hidden'), ('tabgreen', 'Condition category:', 'Condition code:', ''), ('', u'Musculoskeletal', u'Other injuries and accidents', ''), ('', u'Musculoskeletal', u'Normal musculoskeletal and cartilage development and function', ''), ('', 'Description of intervention(s) / exposure:', '* experimental intervention: advice, exercises and passive mobilisations at shoulder region joints', ''), ('Trial_Details_Control_Update_Value_Step1_4', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step1_4', 'Reason:', '', 'hidden'), ('', 'Intervention code:', u'Treatment: Other', ''), ('', 'Comparator / control treatment:', '* control intervention: advice and exercises', ''), ('Trial_Details_Control_Update_Value_Step1_5', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step1_5', 'Reason:', '', 'hidden'), ('', 'Control group:', 'Active', ''), ('Trial_Details_Control_Update_Value_Step1_6', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step1_6', 'Reason:', '', 'hidden'), ('', 'Primary outcome 1:', u'Shoulder Pain and Disability Index (SPADI)', ''), ('', 'Timepoint:', u'1 month and 6 months after randomisation', ''), ('', 'Primary outcome 2:', u'Self-assessed improvement measured on a Likert scale consisting of the following 6 categories: completely recovered; significantly improved; slightly improved; no change; slightly deteriorated; significantly deteriorated', ''), ('', 'Timepoint:', u'1 month and 6 months', ''), ('', 'Secondary outcome:', u'Active abduction and flexion range measured via photography and hand-behind-back range measured using a tape measure.', ''), ('', 'Timepoint:', u'1 month and 6 months', ''), ('', 'Key inclusion criteria:', 'Subjects will be included if they have a unilateral shoulder problem of local mechanical origin. 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Three common treatments for chronic LBP are spinal manipulative therapy, general exercise, and specific stabilisation exercise. While there is evidence that they are effective, to date there has been no head to head comparison of these treatments. We propose to conduct a definitive trial to investigate the effects of these interventions in a population suffering from chronic low back pain.', ''), ('Trial_Details_Control_Update_Value_Step3_10', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_10', 'Reason:', '', 'hidden'), ('', 'Trial website:', '', ''), ('Trial_Details_Control_Update_Value_Step3_11', 'Update:', u'', 'hidden'), ('', 'Presentations / publication list:', '', ''), ('Trial_Details_Control_Update_Value_Step3_12', 'Update:', u'', 'hidden'), ('', 'Name:', 'Dr Jane Latimer', ''), ('Trial_Details_Control_Update_Value_Step3_13', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_13', 'Reason:', '', 'hidden'), ('', 'Address:', 'School of Physiotherapy\nUniversity of Sydney\nPO Box 170\nLidcombe NSW 1825', ''), ('Trial_Details_Control_Update_Value_Step3_14', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_14', 'Reason:', '', 'hidden'), ('', 'Country:', 'Australia', ''), ('Trial_Details_Control_Update_Value_Step3_15', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_15', 'Reason:', '', 'hidden'), ('', 'Tel:', '+61 2 93519191', ''), ('Trial_Details_Control_Update_Value_Step3_16', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_16', 'Reason:', '', 'hidden'), ('', 'Fax:', '', ''), ('Trial_Details_Control_Update_Value_Step3_17', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_17', 'Reason:', '', 'hidden'), ('', 'Email:', 'J.Latimer@fhs.usyd.edu.au', ''), ('Trial_Details_Control_Update_Value_Step3_18', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_18', 'Reason:', '', 'hidden'), ('', 'Name:', 'Associate Professor Chris Maher', ''), ('Trial_Details_Control_Update_Value_Step3_19', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_19', 'Reason:', '', 'hidden'), ('', 'Address:', 'School of Physiotherapy\nUniversity of Sydney\nPO Box 170\nLidcombe NSW 1825', ''), ('Trial_Details_Control_Update_Value_Step3_20', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_20', 'Reason:', '', 'hidden'), ('', 'Country:', 'Australia', ''), ('Trial_Details_Control_Update_Value_Step3_21', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_21', 'Reason:', '', 'hidden'), ('', 'Tel:', '+61 2 93519192', ''), ('Trial_Details_Control_Update_Value_Step3_22', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_22', 'Reason:', '', 'hidden'), ('', 'Fax:', '', ''), ('Trial_Details_Control_Update_Value_Step3_23', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_23', 'Reason:', '', 'hidden'), ('', 'Email:', 'C.Maher@fhs.usyd.edu.au', ''), ('Trial_Details_Control_Update_Value_Step3_24', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_24', 'Reason:', '', 'hidden'), ('', 'Name:', '', ''), ('Trial_Details_Control_Update_Value_Step3_25', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_25', 'Reason:', '', 'hidden'), ('', 'Address:', '', ''), ('Trial_Details_Control_Update_Value_Step3_26', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_26', 'Reason:', '', 'hidden'), ('', 'Country:', '', ''), ('Trial_Details_Control_Update_Value_Step3_27', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_27', 'Reason:', '', 'hidden'), ('', 'Tel:', '', ''), ('Trial_Details_Control_Update_Value_Step3_28', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_28', 'Reason:', '', 'hidden'), ('', 'Fax:', '', ''), ('Trial_Details_Control_Update_Value_Step3_29', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_29', 'Reason:', '', 'hidden'), ('', 'Email:', '', ''), ('Trial_Details_Control_Update_Value_Step3_30', 'Update:', u'', 'hidden'), ('Trial_Details_Control_Update_Reason_Step3_30', 'Reason:', '', 'hidden'), ('', u'', u'', '')] | 83 |
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The primary aim of the study is to determine whether treatment for Obstructive Sleep Apnoea with nasal Continuous Positive Airway Pressure therapy will improve triglyceride metabolism over 24 hours. Triglyceride concentrations in the blood increase after meals and the reduced rate at which they are metabolised is a marker of increased cardiovascular risk. 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March 2014
Run succeeded:
- ran 10 times, most recently for 1 seconds
(0 scraped pages, 0 records)
06:55, 17 March 2014
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May 2011
Edited by
Tim McNamara
9 times
11:43, 11 May 2011
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Difference between, revision and previous revision
Edited by
Tim McNamara
11:00, 11 May 2011