[PDF] Top 20 The ExPeCT (Examining Exercise, Prostate Cancer and Circulating Tumour Cells) trial: study protocol for a randomised controlled trial

... the trial must be obtained from a treating physician involved in ExPeCT ...each study group, the com- puter programme Graphpad will be used to randomly assign a treatment group to each ...the ... See full document

... proposed study is that it is one of the first studies examining a program to increase emotional resilience in a residential setting and is also the only Dutch CBT program specifically adapted to adolescents with ... See full document

... be randomised at the level of the indi- vidual in a 1:1 ratio to either treatment with ...Patients randomised in clinic after a previous diagnostic endoscopy will be started on carvedilol ... See full document

... FOCUS trial is to investigate to what extent CR may improve cognitive abilities and the asso- ciated psychosocial function in patients at UHR for ...we expect that cognitive deficits may be even more ... See full document

... the trial, all clinics will have an attached data clerk responsible for collecting identifiers of all consenting attendees of the chronic disease clinic to allow their identification in the MRC/Wits Agincourt ... See full document

... placebo-controlled, randomised phase II trial of doxycycline 100 mg daily for six weeks in 230 ...be randomised to either oral doxycycline (Azudox®, Kampala Pharmaceutical Industries) 100 mg ... See full document

... SOMNA trial team will assess the potential participant’ s eligibility against the trial inclusion ...meet trial inclusion criteria via telephone, and an inter- view assessment against the ... See full document

... This trial seeks to provide evidence for such an alterna- tive in the form of probiotics, which may increase breastfeeding duration and potentially provide long-term health, cognitive and developmental benefits ... See full document

... previous study where 12 women with >5% uNK cells conceived and 6 subse- quently miscarried (50%) ...endome- trial biopsies (Figure 2). The current on-going pilot study can confirm the presumptions ... See full document

... confirmatory study of aspirin therapy for VLU. AVURT is a phase II randomised, double blind, parallel-group, placebo- controlled study to provide evidence regarding the efficacy and safety of ... See full document

... All randomised participants will receive aspirin or placebo for 24 weeks and will be followed-up for 25 weeks following ...the study, then participants will be asked to inform the study ... See full document

... To ensure retention and to control for contact time, the Health & Wellness (control) arm receives mailed health materials and telephone booster calls at the same fre- quency as the Lifestyle Intervention arm. Mailed ... See full document

... The primary endpoint is the composite endpoint of selected pregnancy- and birth-related complications: PIH, GDM, CS and LGA. PIH and GDM are assessed during pregnancy; CS and LGA are determined at time of delivery (Fig. ... See full document

... Background: Trauma such as hip fracture initiates a neurohumoral stress response that changes the balance between anabolism and catabolism resulting in muscle breakdown and reduced mobilisation. Various studies have ... See full document

... the trial, all clinics will have an attached data clerk responsible for collecting identifiers of all consenting attendees of the chronic disease clinic to allow their identification in the MRC/Wits Agincourt ... See full document

... small randomised controlled trials (RCTs) have produced mixed results with studies suggesting impaired reorientation [33, 34] and improved [35] or unchanged [33] Mini Mental State Examination (MMSE) scores ... See full document

... the trial in keeping with current recommended ...in randomised controlled ...largest trial of over 500 women used "need for an additional uterotonic agent" as the primary out- come ... See full document

... hort study, which showed that continuous intravenous infusion of sedatives was associated with significantly lon- ger mechanical ventilation, increased length of stay in the ICU and in hospital, compared with ... See full document

... the study ’ s Independent Data Monitoring and Ethics Committee (IDMEC), will be performed after an appropriate number of patients have reached the six-month follow-up, to con- firm the final sample ...The ... See full document

... retrospective study, for patients with severe thrombocytopenia, rhTPO could rap- idly increase PCs, reduce 28-day mortality, and there were no severe adverse events during rhTPO ...the study, which was a ... See full document