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The aim of this observational study was to supplement the data on efficacy, safety, and tolerability of telmisartan under daily conditions in hospitals
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with normotension at baseline |
| ||
| Patients with essential hypertension at baseline |
| ||
| Patients with isolated hypertension at baseline |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Telmisartan tablets | Drug | All patients were treated with different doses of telmisartan for 14 days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes from baseline in blood pressure | Evaluation was performed separately for three patient groups depending on their hypertension status at baseline (normotension, essential hypertension and isolated hypertension) | Up to 14 days |
| Number of patients with adverse events | Up to 14 days |
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Inclusion Criteria:
Exclusion Criteria: Not applicable
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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| ID | Term |
|---|---|
| D000077333 | Telmisartan |
| ID | Term |
|---|---|
| D001713 | Biphenyl Compounds |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
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|
| D006838 |
| Hydrocarbons |
| D009930 | Organic Chemicals |
| D001562 | Benzimidazoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |