The Trial
The Belgian trial with azithromycin for acute COPD exacerbations requiring hospitalization: an investigator-initiated study protocol for a multicenter, randomized, double-blind, placebo-controlled trial
... BACE trial is funded by a grant from the Agentsc- hap voor Innovatie door Wetenschap en Technologie (IWT) through the Toegepast Biomedisch onderzoek met een primair Maatschappelijke finaliteit (TBM) program: ...
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Single-center, noninterventional clinical trial to assess the safety, efficacy, and tolerability of a dimeticone-based medical device in facilitating the removal of scales after topical application in patients with psoriasis corporis or psoriasis capitis
... The trial col- lective involved patients who were eligible for the intended use of the product because of their degree of symptoms in the opinion of the responsible physician or dermatologist and who met the ...
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Protocol for a multicentre randomised feasibility STUdy evaluating the impact of a prognostic model for Management of BLunt chest wall trauma patients: STUMBL trial.
... the trial if they present to the ED with isolated blunt chest wall trauma, are aged ≥18 and are capable of giving consent to ...the trial if they lose capacity (including death) to complete the surveys and ...
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THE CRITICAL READING AND THINKING ABILITIES OF MALAY SECONDARY SCHOOL PUPILS IN SINGAPORE
... The objectives of the trial run were to validate and to establish the reliability of the two trial instruments of the study, namely, the Trial Malay Language Critical Reading Test (TMLCR[r] ...
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A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD: the DuoSleep study
... For the crossover design, a paired t-test was used for the sample size calculation with a mean difference of 2, SD of 3.8, and a significance level of 0.05. A Δ of 2 (change in nighttime oxygenation in percent) was ...
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<p>The Relationship Between Clinical Trial Participation and Inhaler Technique Errors in Asthma and COPD Patients</p>
... clinical trial experience and inhaler adequacy may be confounded by the differential inclusion of participants with adequate technique into clinical ...the trial. The limited access to clinical trial ...
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Reasons for participating in randomised controlled trials: conditional altruism and considerations for self
... REFLUX trial was primarily a RCT, it also included parallel non-randomised patient prefer- ence groups in recognition that the marked differences in the treatments were likely to make the choice between them ...
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Therapeutic options for chronic inflammatory demyelinating polyradiculoneuropathy: a systematic review
... Three randomised controlled clinical trials studying the efficacy and safety of IVIg were identified and included in the review (Table 1). Leger et al. [24] undertook a double- blind, placebo controlled crossover study ...
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A controlled, randomized nonblinded clinical trial to assess the efficacy of amphotericin B deoxycholate as compared to pentamidine for the treatment of antimony unresponsive visceral leishmaniasis cases in Bihar, India
... facilities and is a recognized specialized treatment centre for Kala-azar. Generally, patients are referred from vari- ous primary health centers and district hospitals with their earlier treatment records to RMRIMS in ...
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The ADOPT trial (<u>A</u>ssessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/<u>D</u>) f<u>o</u>r Heart Failure <u>P</u>atients in China): rationale, design, and end-points
... Since a large proportion of the population in China is not covered by health insurance, many CHF patients cannot afford CRT, and thus have to choose optimal pharmaceuti- cal therapy (OPT) instead of CRT. For this reason ...
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Clinical trial design in the era of comparative effectiveness research
... the trial. A pragmatic/effectiveness trial is designed to determine the effectiveness of an intervention in a real-world setting and will include a broad spectrum of ...The trial will be embedded in ...
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Sex dependency of inhibitory control functions
... stop trial, the participants’ response time increased in the following go trial and ap- peared as post-error slowing or post-stop slowing, re- ...stop trial slowing might reflect a momentary shift of ...
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Changes in CVD risk factors in the activity counseling trial
... The investigators express their appreciation to ACT- participating physicians and other health professionals, participating patients, and the Data and Safety Monitoring Board, whose members were Albert Oberman (Chair), ...
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<p>A randomized controlled trial evaluating the effects of amlodipine on myocardial iron deposition in pediatric patients with thalassemia major</p>
... controlled trial with allocation of a 1:1 ...clinical trial registry number is PACTR201902478249291. The trial was conducted in accordance with the Declaration of ...
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<p>Cost-effectiveness of the COPD Patient Management European Trial home-based disease management program</p>
... The trial was approved by the local or national ethics committees and competent authority per country for each investigational center where applicable, and all patients provided written, informed consent (Table ...
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“I didn’t really understand it, I just thought it’d help”: exploring the motivations, understandings and experiences of patients with advanced lung cancer participating in a non placebo clinical IMP trial
... non-placebo trial design add the following more specific reasons for in-depth, qualitative investigation of patient perspectives and experiences in this and other similar ...the trial or intervention ...
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‘We all want to succeed, but we’ve also got to be realistic about what is happening’: an ethnographic study of relationships in trial oversight and their impact
... the trial succeeding ...the trial was in crisis, CTU staff were perceived as more objective and hence able to see if a trial faced intractable ...the trial team mem- ber and the trial: ...
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The COLOFOL trial: study design and comparison of the study population with the source cancer population
... the trial was restricted to patients #75 years of age with a life expectancy exceeding 2 years based on concomi- tant ...the trial was approved by the ethical committee of Uppsala University, 2004: M-453 ...
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Detailed statistical analysis plan for the pulmonary protection trial
... Linear mixed-effects model analysis of longitudinal data will be used to analyze the primary outcome. The linear mixed-effects model approach handles missing data appropriately and we will therefore not use multiple ...
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<p>The LipiDiDiet trial: what does it add to the current evidence for Fortasyn Connect in early Alzheimer’s disease?</p>
... Preventive Trial (MAPT), 32 have evaluated combinations of interventions that affect risk factors for AD ...the trial ’ s outcomes (although the use of omega-3 preparations, and the intake of folic acid and ...
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