Hypertension
Conditions
Keywords
VALSARTAN, HYDROCHLOROTHIAZIDE, OLMESARTAN, HYPERTENSION
Brief summary
To evaluate the efficacy of valsartan 160 mg/HCTZ 25 mg in patients not adequately responding to monotherapy with olmesartan medoxomil 40 mg or combination therapy with olmesartan medoxomil 20 mg plus HCTZ 12.5 mg by testing the hypothesis that valsartan 160 mg/HCTZ 25 mg significantly reduces the trough mean sitting diastolic blood pressure (MSDBP) after a 4-week treatment in the nonresponder population.
Interventions
Sponsors
Novartis
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
* Females must be either post-menopausal for one year, surgically sterile or using effective contraceptive methods (e.g. barrier method with spermicide, intra-uterine device, hormonal contraceptives). * Patients with essential hypertension: * At Visit 1, untreated patients should have a MSDBP \>100 mmHg and \< 110 mmHg and treated patients need to have a MSDBP \< 110 mmHg. Untreated patients can be included as soon as the safety laboratory parameters are available, but not at the day of Visit 1. This inclusion visit will be recorded as Visit 3 in the CRF. * At Visit 2, patients previously treated for hypertension need to have a MSDBP ≥ 100 mmHg and \< 110 mmHg for entrance into the first treatment phase. Patients previously treated for hypertension who have a MSDBP \< 100 mmHg at Visit 2 will continue the wash-out phase and will be again evaluated with regard to BP criteria at Visit 3. Untreated patients do not perform Visit 2. * At Visit 3, which is not performed for patients who entered the first treatment phase already at Visit 2, patients need to have a MSDBP \>100 mmHg and \< 110 mmHg for entrance into the first treatment phase. * At Visit 4, all patients need to have a MSDBP \>90 mmHg for entrance into the second treatment phase.
Exclusion criteria
* MSDBP \>110 mmHg or MSSBP \>180 mmHg * Pregnant or nursing women * Inability to completely discontinue all antihypertensive medications safely for a period of up to 2 weeks, as required by the protocol Other protocol-defined
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from baseline in diastolic blood pressure after 4 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Change from baseline in systolic blood pressure after 4 weeks | — |
| Diastolic blood pressure less than 90 mmHg after 4 weeks | — |
| Diastolic blood pressure less than 90 mmHg or decrease in diastolic blood pressure of 10 mmHg or greater after 4 weeks | — |
| Change from baseline heart rate after 4 weeks | — |
Countries
Germany, Switzerland
Outcome results
None listed