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Table 1 Number of selected studies on paediatric MS and CJD meeting specific criteria

From: Systematic reviews in paediatric multiple sclerosis and Creutzfeldt-Jakob disease exemplify shortcomings in methods used to evaluate therapies in rare conditions

  RCT Clinical endpoints Prospective analysis Sample size calculation Adjustments for multiple testing Confounding addressed Industry sponsored
Paediatric MS (n = 12) 1 12 6 1 1 2 3
CJD (n = 7) 3 7 5 4 0 4 1