Table 3.
Drug 1 | Drug 2 | |||
---|---|---|---|---|
Trial 1 (N = 100,000) | Trial 2 (N = 52,963) | Trial 1 (N = 100,000) | Trial 2 (N = 52,963) | |
Control group: Rc | 0.351 | 0.195 | 0.351 | 0.195 |
Treated group: Rt | 0.089 | 0.029 | 0.335 | 0.181 |
Efficacy metrics | ||||
OR | 0.358 | 0.181 | 0.978 | 0.945 |
RR | 0.255 | 0.150 | 0.955 | 0.929 |
AB | 0.261 | 0.166 | 0.016 | 0.014 |
NNT | 4 | 6 | 63 | 72 |
In trial 1, the whole population was included as it was not possible to include a randomised sample because the approach does not take into consideration random variations and, thus, confidence intervals. In trial 2, a non-randomised sample was selected, with a lower average risk in the untreated patients than that for the whole population
AB absolute benefit, N trial population size, NNT number needed to treat, OR odds ratio, Rc risk in control group, RR relative risk, Rt risk in treated group