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. Author manuscript; available in PMC: 2017 Aug 7.
Published in final edited form as: Int J Obes (Lond). 2016 Apr 26;40(7):1043–1050. doi: 10.1038/ijo.2016.69

Table 2. Suggestions regarding target population and eligibility.

  • Age: 12-17 years old (once safety/efficacy is established in this age-group, trials of younger children can be initiated)

  • BMI ≥95th percentile (depending upon the risk/benefit of the agent(s) under investigation, requirement of ≥1 co-morbid condition may be appropriate)

  • Tanner stage: no lower limit unless evidence suggests developmental risk of specific agent

  • No upper BMI threshold (can consider sub-analyses by BMI categories)

  • Include participants taking potentially weight altering medication(s) with stable dose for ≥6 months

  • Observed or documented history of failed weight loss attempts unnecessary