Compared to placebo, the reduction in the primary efficacy endpoint at one month with atomoxetine barely missed statistical significance ( P = 0.053); however, atomoxetine significantly reduced the primary efficacy endpoint after three months ( P < 0.001).
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Atomoxetine as an adjunct to nonpharmacological treatments for preventing vasovagal attacks in patients with recurrent vasovagal syncope: A pilot randomized-controlled trial.
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0.0530
0.0530