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Bisoprolol Adverse Reaction clinical trials

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NCT ID: NCT04432610 Withdrawn - Clinical trials for Nebivolol Adverse Reaction

Echocardiographic Study of a Single Dose Bisoprolol Versus Nebivolol in Healthy Subjects

BINEB
Start date: January 2030
Phase: Phase 4
Study type: Interventional

This is a randomized, double-blind, crossover study in healthy adult subjects. Each subject will receive a single dose of bisoprolol 5 mg p.o. and nebivolol 5 mg p.o. with 1 week washout period. All subjects will undergo a physical examination, 12-lead electrocardiography and a comprehensive echocardiographic study before the administration of the study drug and 5 hours thereafter.