Hypertension
Conditions
Brief summary
The aim of the observational study was to supplement the data on efficacy, safety and tolerability of telmisartan under daily conditions in hospitals
Interventions
DRUGTelmisartan
Sponsors
Boehringer Ingelheim
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients with diagnosis of essential hypertension * Minimum age of 18 years
Exclusion criteria
* NA
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in clinic blood pressure | up to 14 days |
| Number of patients with adverse drug reactions | up to 14 days |
Outcome results
None listed