The 20 mg group had a higher responder rate (odds ratio 2.13, 95% CI 0.96, 4.69) and % change in seizure frequency over placebo (win odds 1.30, 95% CI 0.98, 1.73) which did not reach statistical significance; however, adverse events were worse than placebo in the 20 mg group (win odds 0.69, 95% CI 0.51, 0.94) and thus the Epilepsy‐DOOR showed no benefit over placebo (win odds 0.98, 95% CI 0.71, 1.35).
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The Epilepsy-Desirability of Outcome Ranking (DOOR) as a Multi-Faceted Consumer-Informed Outcome Measure for Epilepsy Clinical Trials.
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