首页> 外文期刊>Trials >Multi-dose Oral Ondansetron for Pediatric Gastroenteritis: study Protocol for the multi-DOSE oral ondansetron for pediatric Acute GastroEnteritis (DOSE-AGE) pragmatic randomized controlled trial
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Multi-dose Oral Ondansetron for Pediatric Gastroenteritis: study Protocol for the multi-DOSE oral ondansetron for pediatric Acute GastroEnteritis (DOSE-AGE) pragmatic randomized controlled trial

机译:多剂量口服ondansetron用于儿科胃肠炎:用于多剂量口服ondansetron的研究方案,用于小儿急性胃肠炎(剂量症)务实随机对照试验

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BACKGROUND:There are limited treatment options that clinicians can provide to children presenting to emergency departments with vomiting secondary to acute gastroenteritis. Based on evidence of effectiveness and safety, clinicians now routinely administer ondansetron in the emergency department to promote oral rehydration therapy success. However, clinicians are also increasingly providing multiple doses of ondansetron for home use, creating unquantified cost and health system resource use implications without any evidence to support this expanding practice.METHODS/DESIGN:DOSE-AGE is a randomized, placebo-controlled, double-blinded, six-center, pragmatic clinical trial being conducted in six Canadian pediatric emergency departments (EDs). In September 2019 the study began recruiting children aged 6?months to 18?years with a minimum of three episodes of vomiting in the 24 h preceding enrollment, 72?h of gastroenteritis symptoms and who were administered a dose of ondansetron during their ED visit. We are recruiting 1030 children (1:1 allocation via an internet-based, third-party, randomization service) to receive a 48-h supply (i.e., six doses) of ondansetron oral solution or placebo, administered on an as-needed basis. All participants, caregivers and outcome assessors will be blinded to group assignment. Outcome data will be collected by surveys administered to caregivers 24, 48 and 168 h following enrollment. The primary outcome is the development of moderate-to-severe gastroenteritis in the 7?days following the ED visit as measured by a validated clinical score (the Modified Vesikari Scale). Secondary outcomes include duration and frequency of vomiting and diarrhea, proportions of children experiencing unscheduled health care visits and intravenous rehydration, caregiver satisfaction with treatment and safety. A preplanned economic evaluation will be conducted alongside the trial.DISCUSSION:Definitive data are lacking to guide the clinical use of post-ED visit multidose ondansetron in children with acute gastroenteritis. Usage is increasing, despite the absence of supportive evidence. The incumbent additional costs associated with use, and potential side effects such as diarrhea and repeat visits, create an urgent need to evaluate the effect and safety of multiple doses of ondansetron in children focusing on post-emergency department visit and patient-centered outcomes.TRIAL REGISTRATION:ClinicalTrials.gov: NCT03851835. Registered on 22 February 2019.
机译:背景:临床医生可以提供有限的治疗方案,临床医生可以向儿童提供给急诊部门的儿童,呕吐继发于急性胃肠炎。基于有效性和安全的证据,临床医生现在经常在急诊部门举行ondansetron以促进口服补液治疗成功。然而,临床医生也越来越多地为家庭使用提供多剂ondansetron,创造了无需资金和健康系统资源使用的影响,没有任何证据支持这种扩展的做法。方法/设计:剂量为期,是一个随机的,安慰剂控制的双重盲目的,六个中心,六个加拿大儿科急诊部门(EDS)进行了务实的临床试验。 2019年9月,该研究开始招募6岁的儿童6个月至18岁的儿童,最少三个呕吐在前列报名前的胃肠炎症状<72?H期间在入场期间举办一剂ondansetron of ondansetron。 。我们正在招聘1030名儿童(通过基于互联网,第三方,随机化服务),以获得48-H供应(即,六个剂量)的ondansetron口服解决方案或安慰剂,按照必要的基础管理。所有参与者,护理人员和结果评估员将被蒙蔽对团体分配。结果数据将通过管理在入学后给予护理人员24,48和168小时的调查收集。主要结果是在通过验证的临床评分(改进的Vesikari Scale)测量后,在ED访问后7天在7日内进行中度至严重的胃肠炎的发展。二次结果包括呕吐和腹泻的持续时间和频率,儿童的比例,经历了不受治金的医疗保健访问和静脉注重,护理人员满意治疗和安全。将与试用期间进行审慎的经济评估。探讨:缺乏明确的数据,以指导急性胃肠炎儿童在儿童中的临床用途。尽管没有支持证据,但使用情况正在增加。与使用相关的现任额外成本以及腹泻和重复访问等潜在的副作用,迫切需要评估多剂量ondansetron在专注于急诊后部的儿童访问和患者以患者为中心的结果的效果和安全性.TRIAL注册:ClinicalTrials.gov:NCT03851835。 2019年2月22日注册。

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