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A double blind study to examine the safety and efficacy of different dosages of lercanidipine in normal weight and obese patients with hypertension
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lercanidipine | Drug |
| Measure | Description | Time Frame |
|---|---|---|
| change from baseline of systolic blood pressure (BPs) after 4 weeks of treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Blood pressure, response rate, normalization rate, pulse rate, lipid profile, safety and tolerability. Measures after 4, 8, 12 weeks. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jürgen Scholze, MD | UCB Pharma | Study Director |
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| ID | Term |
|---|---|
| D006973 | Hypertension |
| D009765 | Obesity |
| ID | Term |
|---|---|
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D050177 | Overweight |
| D044343 | Overnutrition |
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| ID | Term |
|---|---|
| C060343 | lercanidipine |
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| D009748 |
| Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
| D001835 | Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |