Hypertension
Conditions
Brief summary
A study to evaluate the effects of combination losartan versus combination atenolol in patients with ambulatory systolic hypertension.
Interventions
DRUGMK0954, losartan potassium/Duration of Treatment: 18 weeks
DRUGComparator: losartan, HCTZ, amlodipine, atenolol/Duration of Treatment: 18 weeks
Sponsors
Organon and Co
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Males or females at least 18 years of age who have ambulatory systolic hypertension.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean daytime ambulatory systolic blood pressure | — |
Secondary
| Measure | Time frame |
|---|---|
| Ambulatory BP | — |
| Pulse pressure | — |
| Trough sitting BP | — |
| Percentage of patients who reach goal ambulatory systolic BP | — |
Outcome results
None listed