drugset / Trial / NCT02612298

Efficacy and Safety of Arotinolol Hydrochloride on Morning Blood Pressure and Heart Rate

NCT02612298

Phase 4 Completed 198 enrolled Marubeni Pharmaceuticals (Suzhou) Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the efficacy and safety of Arotinolol Hydrochloride and Metoprolol succinate on morning blood pressure, heart rate and target organ damage in patients with essential hypertension. To provide evidence for hypertension treatment. A group: Arotinolol Hydrochloride, oral, 5-15mg, bid for 12 weeks. B group: Metoprolol succinate sustained-release tablet, oral, 23.75-71.25mg, qd for 12 weeks.

Timeline

Start
2015-08
Primary completion
2018-09-13
Completion
2018-09-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Arotinolol Small molecule 5 mg Oral
Subject Arotinolol Small molecule 15 mg Oral
Comparator Metoprolol Other / unclassified 23.75 mg Oral
Comparator Metoprolol Other / unclassified 71.25 mg Oral