| Literature DB >> 25711607 |
Beth D Kirkpatrick1, E Ross Colgate1, Josyf C Mychaleckyj2, Rashidul Haque2, Dorothy M Dickson2, Marya P Carmolli2, Uma Nayak2, Mami Taniuchi2, Caitlin Naylor2, Firdausi Qadri2, Jennie Z Ma2, Masud Alam2, Mary Claire Walsh2, Sean A Diehl2, William A Petri2.
Abstract
Oral vaccines appear less effective in children in the developing world. Proposed biologic reasons include concurrent enteric infections, malnutrition, breast milk interference, and environmental enteropathy (EE). Rigorous study design and careful data management are essential to begin to understand this complex problem while assuring research subject safety. Herein, we describe the methodology and lessons learned in the PROVIDE study (Dhaka, Bangladesh). A randomized clinical trial platform evaluated the efficacy of delayed-dose oral rotavirus vaccine as well as the benefit of an injectable polio vaccine replacing one dose of oral polio vaccine. This rigorous infrastructure supported the additional examination of hypotheses of vaccine underperformance. Primary and secondary efficacy and immunogenicity measures for rotavirus and polio vaccines were measured, as well as the impact of EE and additional exploratory variables. Methods for the enrollment and 2-year follow-up of a 700 child birth cohort are described, including core laboratory, safety, regulatory, and data management practices. Intense efforts to standardize clinical, laboratory, and data management procedures in a developing world setting provide clinical trials rigor to all outcomes. Although this study infrastructure requires extensive time and effort, it allows optimized safety and confidence in the validity of data gathered in complex, developing country settings. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2015 PMID: 25711607 PMCID: PMC4385767 DOI: 10.4269/ajtmh.14-0518
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345