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Study of the efficacy and tolerance of Motens® (lacidipine) in patients with essential hypertension. To obtain information on the dosage used in practice and the tolerance at the start of treatment (12 weeks)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Motens |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Motens® (lacidipine) | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Assessment of efficacy by the investigator on a 4-point verbal rating scale based on changes in blood pressure | Up to 12 weeks after start of drug administration | |
| Assessment of tolerability by investigator on a 4-point verbal rating scale | Up to 12 weeks after start of drug administration | |
| Number of patients with adverse events | Up to 12 weeks after start of drug administration |
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Inclusion Criteria:
Non-hospitalised patients of both sexes aged 18 years or more with essential hypertension requiring treatment according to the recommendations of the German League for Hypertension
Exclusion Criteria:
Patients who had the contraindications listed in the product information (the case report file contained a copy of the product information)
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Patients with essential Hypertension recruited by General practicioners, cardiologists and specialists in internal medicine in non-Hospital practice
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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| ID | Term |
|---|---|
| C060285 | lacidipine |
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