Large Pediatric Randomized Clinical Trials in ClinicalTrials.gov

Author:

Cho Stephanie M.1,Serghiou Stylianos23,Ioannidis John PA.123,Klassen Terry P.4,Contopoulos-Ioannidis Despina G.5

Affiliation:

1. Stanford Prevention Research Center, Department of Medicine, Stanford University School of Medicine, Stanford, California94305

2. Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, California; 94305

3. Meta-Research Innovation Center at Stanford (METRICS), Stanford University, Stanford, California; 94305

4. Department of Pediatrics and Child Health, University of Manitoba and Children’s Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada

5. Division of Infectious Diseases, Department of Pediatrics, Stanford University School of Medicine, Stanford, California

Abstract

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 Few trials (18%; 44 of 247) targeted mortality as an outcome. 35% (58 of 164) of the trials completed ≥12 months were unpublished at the time of our assessment.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 (ρ = 0.76) and in LMICs (ρ = 0.69), but not in HICs (ρ = 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.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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