Large Pediatric Randomized Clinical Trials in ClinicalTrials.gov

被引:3
|
作者
Cho, Stephanie M. [1 ]
Serghiou, Stylianos [2 ,3 ]
Ioannidis, John Pa [1 ,2 ,3 ]
Klassen, Terry P. [4 ,5 ]
Contopoulos-Ioannidis, Despina G. [6 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94304 USA
[2] Stanford Univ, Dept Epidemiol & Populat Hlth, Sch Med, Stanford, CA 94304 USA
[3] Stanford Univ, Metares Innovat Ctr, Stanford METRICS, Stanford, CA 94304 USA
[4] Univ Manitoba, Dept Pediat & Child Hlth, Winnipeg, MB, Canada
[5] Childrens Hosp Res Inst Manitoba, Winnipeg, MB, Canada
[6] Stanford Univ, Dept Pediat, Sch Med, Div Infect Dis, Stanford, CA 94304 USA
关键词
GLOBAL BURDEN; CHILDREN; DISEASE; DISABILITY;
D O I
10.1542/peds.2020-049771
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: Large, randomized controlled trials (RCTs) are essential in answering pivotal questions in child health. METHODS: We created a bird's eye view of all large, noncluster, nonvaccine pediatric RCTs with >= 1000 participants registered in ClinicalTrials.gov (last search January 9, 2020). We analyzed the funding sources, countries, outcomes, publication status, and correlation with the pediatric global burden of disease (GBD) for eligible trials. RESULTS: We identified 247 large, nonvaccine, noncluster pediatric RCTs. Only 17 mega-trials with >= 5000 participants existed. Industry funding was involved in only 52 (21%) and exclusively funded 47 (19%) trials. Participants were from high-income countries (HICs) in 100 (40%) trials, from lower-middle-income countries (LMICs) in 122 (49%) trials, and from both HICs and LMICs in 19 (8%) trials; 6 trials did not report participants' country location. Of trials conducted in LMIC, 43% of investigators were from HICs. Of non-LMIC participants trials (HIC or HIC and LMIC), 39% were multicountry trials versus 11% of exclusively LMIC participants trials. Few trials (18%; 44 of 247) targeted mortality as an outcome. 35% (58 of 164) of the trials completed >= 12 months were unpublished at the time of our assessment. The number of trials per disease category correlated well with pediatric GBD overall (rho = 0.76) and in LMICs (rho = 0.69), but not in HICs (rho = 0.29). CONCLUSIONS: Incentivization of investigator collaborations across diverse country settings, timely publication of results of large pediatric RCTs, and alignment with the pediatric GBD are of pivotal importance to ultimately improve child health globally.
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页数:51
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