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首页> 外文期刊>The American heart journal >Characteristics of pediatric cardiovascular clinical trials registered on ClinicalTrials.gov
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Characteristics of pediatric cardiovascular clinical trials registered on ClinicalTrials.gov

机译:在ClinicalTrials.gov上注册的小儿心血管临床试验的特征

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Background ClinicalTrials.gov is an National Institutes of Health-sponsored registry of federally and privately funded trials. We sought to determine fundamental characteristics of registered pediatric cardiovascular trials (PCVTs). Methods A data set including 68,134 interventional clinical trials was downloaded from ClinicalTrials.gov and entered into a relational database. Aggregate data from PCVTs were compared with other trial specialties. Multivariable logistic regression was used to evaluate factors associated with improved trial quality metrics including blinding and randomization. Results Between July 1, 2005, and September 27, 2010, 5035 (7%) registered trials targeted pediatric populations, including 213 PCVTs (4.2%), 1,176 pediatric infectious disease trials (23%), 664 pediatric mental health trials (13%), and 346 pediatric hematology/oncology trials (7%). Median (interquartile range) PCVT enrollment was 65 subjects (36-186) and median study duration was 2.3 years (1.3-3.7). The most common PCVTs targeted acquired diseases including hypertension (n = 41, 14%), obesity (n = 26, 9%), pulmonary hypertension (n = 25, 9%), and dyslipidemia (n = 19, 7%). Important factors associated with improved quality metrics included National Institutes of Health as opposed to industry funding (OR, 1.9; P <.0001); trial location (trials with both US and foreign enrollment vs trials with US only or foreign only enrollment, P =.02) and trials restricted to younger children as opposed to trials including adolescents (OR, 1.4; P <.0001). Conclusion PCVTs represent a small proportion of clinical trials relative to other pediatric subspecialties. Most PCVTs tend to parallel adult morbidities while there is a relative paucity of trials focused on congenital heart disease. These data may be useful to stakeholders in informing decisions regarding the conduct of PCVTs, and to provide insight into mechanisms to advance PCVT infrastructure.
机译:背景ClinicalTrials.gov是由美国国立卫生研究院(National Institutes of Health)赞助的联邦和私人资助试验注册机构。我们试图确定已注册的儿科心血管试验(PCVT)的基本特征。方法从ClinicalTrials.gov下载包括68,134项介入性临床试验的数据集,并将其输入关系数据库。将PCVT的汇总数据与其他试验专业进行了比较。多变量logistic回归用于评估与改善的试验质量指标相关的因素,包括盲法和随机化。结果2005年7月1日至2010年9月27日之间,针对儿童人群的注册试验为5035(7%),包括213例PCVT(4.2%),1,176例儿童传染病试验(23%),664例儿童心理健康试验(13% )和346项儿科血液学/肿瘤学试验(7%)。 PCVT的中位(四分位间距)为65名受试者(36-186),中位研究持续时间为2.3年(1.3-3.7)。最常见的PCVT以获得性疾病为目标,包括高血压(n = 41,14%),肥胖症(n = 26,9%),肺动脉高压(n = 25,9%)和血脂异常(n = 19,7%)。与改善质量指标相关的重要因素包括国立卫生研究院,而不是行业资助(OR,1.9; P <.0001);审判地点(美国和外国入学的审判与仅美国或仅外国入学的审判,P = .02)以及仅限于年幼儿童的审判,而不是包括青少年在内的审判(OR,1.4; P <.0001)。结论相对于其他儿科亚专业,PCVT占临床试验的一小部分。大多数PCVT往往与成人发病率平行,而针对先天性心脏病的试验相对较少。这些数据对于利益相关者在通知有关PCVT行为的决策时可能有用,并有助于深入了解促进PCVT基础结构的机制。

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