70
Participants
Start Date
March 31, 2012
Primary Completion Date
March 31, 2016
Study Completion Date
March 31, 2016
Nebivolol
Doses will be titrated based on weekly visits during the first 2 weeks to achieve a target SBP\<140 and DBP \<90 mm Hg. If BP remains uncontrolled after 2 weeks of treatment, indapamide will be added at a dosage of 2.5 mg/day. If the therapeutic goal is still not achieved by 4 weeks, patients will be withdrawn from the study.Upward titration will be halted, and the previous dosage level resumed, if at any point systolic blood pressure falls to ≤ 100 mmHg, even if the individual remains asymptomatic.
Icahn School of Medicine at Mount Sinai, New York
Collaborators (1)
Forest Laboratories
INDUSTRY
Icahn School of Medicine at Mount Sinai
OTHER