This study will evaluate the efficacy and safety of nebivolol monotherapy in Hispanic patients with stage 1 or stage 2 hypertension
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
277
Nebivolol 5 mg, 5-mg Nebivolol nontrade tablets , oral administration Nebivolol 10 mg, 10-mg Nebivolol nontrade tablets , oral administration Nebivolol 20 mg, 20-mg Nebivolol nontrade tablets , oral administration Nebivolol 40 mg, two 20-mg Nebivolol nontrade tablets , oral administration
Matching placebo tablets, oral administration
Change From Baseline in Trough Seated DBP at Week 8(LOCF).
The primary efficacy parameter was the change from baseline in mean trough seated DBP at Week 8. The average of three consecutive BP measurements would be the mean trough seated DBP value.
Time frame: From baseline visit 7 (week 0) to end of double-blind treatment phase visit 11 (week 8)
Change From Baseline in Trough Seated Systolic Blood Pressure (SBP) at Week 8 (LOCF).
The secondary efficacy parameter was the change from baseline in mean trough seated SBP at Week 8. The average of three consecutive BP measurements would be the mean trough seated SBP value.
Time frame: From baseline visit 7 (week 0) to end of double-blind treatment phase visit 11 (week 8)
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Forest Investigative Site
Buena Park, California, United States
Forest Investigative Site
Chino, California, United States
Forest Investigative Site
Long Beach, California, United States
Forest Investigative Site
Los Angeles, California, United States
Forest Investigative Site
National City, California, United States
Forest Investigative Site
San Bernardino, California, United States
Forest Investigative Site
Temecula, California, United States
Forest Investigative Site
Tustin, California, United States
Forest Investigative Site
Coral Gables, Florida, United States
Forest Investigative Site FL2
Hialeah, Florida, United States
...and 22 more locations