drugset / Trial / NCT01066039

Phase 4 Study to Assess the Effect of Bisoprolol on Glycemic Level in Type II Diabetic Subjects With Suboptimal Blood Pressure Control

NCT01066039

Phase 4 Completed 202 enrolled Merck KGaA, Darmstadt, Germany Merck Ltd. · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a 24-week, prospective, multicenter, open-label, single-arm study to assess the effect of bisoprolol on glycemic level in Type 2 diabetes mellitus (T2DM) controlled subjects with hypertension. The hypothesis of study is that there is no change in glycemic level and lipid metabolism as determined by glycosylated hemoglobin (HbA1c) using bisoprolol in T2DM subjects with suboptimal blood pressure (BP) control.

Timeline

Start
2010-04
Primary completion
2013-04
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Bisoprolol Other / unclassified 2.5 mg Oral
Subject Bisoprolol Other / unclassified 5 mg Oral
Subject Bisoprolol Other / unclassified 10 mg Oral