Trial Characteristics That Affect Parental Consent in Neonatal Drug Trials

Hanvey I. Blaire; Aliaga Sofia; Laughon Matthew M.; Testoni Daniela; Smith P. Brian; Bauserman Melissa

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Trial Characteristics That Affect Parental Consent in Neonatal Drug Trials

机译：在新生药试验中影响父母同意的试验特征

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Objective The main purpose of this article is to determine parental consent rates in neonatal drug trials and describe trial characteristics associated with higher rates.

机译：目的本文的主要目的是确定新生药试验中的父母同意率，并描述与更高率相关的试验特征。

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来源
《American Journal of Perinatology》 |2019年第7期|共6页
作者
Hanvey I. Blaire; Aliaga Sofia; Laughon Matthew M.; Testoni Daniela; Smith P. Brian; Bauserman Melissa;
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作者单位

Univ N Carolina Sch Med Dept Pediat Chapel Hill NC 27515 USA;

Univ N Carolina Sch Med Dept Pediat Chapel Hill NC 27515 USA;

Univ N Carolina Sch Med Dept Pediat Chapel Hill NC 27515 USA;

Univ Fed Sao Paulo Escola Paulista Med Sao Paulo Brazil;

Duke Univ Med Ctr Dept Pediat Durham NC 27710 USA;

Univ N Carolina Sch Med Dept Pediat Chapel Hill NC 27515 USA;

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原文格式 PDF
正文语种 eng
中图分类产科学;
关键词
newborn; clinical trial; parental consent; informed consent;

机译：新生儿;临床试验;父母同意;知情同意;

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专利

1. Trial Characteristics That Affect Parental Consent in Neonatal Drug Trials [J] . Hanvey I. Blaire, Aliaga Sofia, Laughon Matthew M., American Journal of Perinatology . 2019,第7期

机译：在新生药试验中影响父母同意的试验特征
2. Fifteen-minute consultation: an evidence-based approach to research without prior consent (deferred consent) in neonatal and paediatric critical care trials [J] . Woolfall Kerry, Frith Lucy, Dawson Angus, Archives of disease in childhood. Education and practice edition . 2016,第1期

机译：15分钟咨询：新生儿和儿科重症监护试验中未经事先同意（延期同意）的循证研究方法
3. Parental Decision-Making Processes in Pediatric Trial Enrollment: Recommendations for Informed Consent in Genetic Eye Disease Research for Cell Therapies [J] . Brooks Stephanie, Bubela Tania Investigative ophthalmology & visual science . 2018,第9期

机译：儿科审判入学育儿决策过程：关于细胞疗法遗传眼病研究的知情同意的建议
4. CHARACTERISTICS OF DRUG COMBINATION THERAPY IN ONCOLOGY BY ANALYZING CLINICAL TRIAL DATA ON CLINICALTRIALS.GOV [C] . MENGHUA WU, MARINA SIROTA, ATUL J.BUTTE, Pacific Symposium on Biocomputing . 2015

机译：通过分析临床试验数据临床试验数据的临床药物组合治疗的特征.GOV
5. Rethinking Informed Consent Requirements for Pragmatic Comparative Effectiveness Trials [D] . Whicher, Danielle. 2014

机译：对务实比较有效性试验的知情同意要求的重新思考
6. Improved parental understanding by an enhanced informed consent form: a randomized controlled study nested in a paediatric drug trial [O] . Nut Koonrungsesomboon, Chanchai Traivaree, Charnunnut Tiyapsane, 2019

机译：通过增强的知情同意书形式改善父母的理解：一项在儿科药物试验中嵌套的随机对照研究
7. Parental and professional perceptions of informed consent and participation in a time-critical neonatal trial: a mixed-methods study in India, Sri Lanka and Bangladesh [O] . Stuti Pant, Maya Annie Elias, Kerry Woolfall, 2021

机译：父母和专业知识的知情同意和参与时间关键的新生儿试验：印度的混合方法研究，斯里兰卡和孟加拉国

Trial Characteristics That Affect Parental Consent in Neonatal Drug Trials

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