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| Study Type: | Observational |
|---|---|
| Study Design: | Prospective |
| Condition: |
Hypertension |
Participant Flow
| Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations |
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| Significant events and approaches for the overall study following participant enrollment, but prior to group assignment |
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| Description | |
|---|---|
| Hypertensive Patients With Micardis Plus for the First Time | In Post Marketing Surveillance (PMS), there are totally three figures. The number of enrolled patients: 6,901/ The number of patients for safety assessment: 6,606/ The number of patients for efficacy assessment: 6,120. |
| Hypertensive Patients With Micardis Plus for the First Time | |
|---|---|
| STARTED | 6901 |
| COMPLETED | 6120 |
| NOT COMPLETED | 781 |
| Micardis+ before the date of contract | 201 |
| duplicated subjects | 68 |
| no start date of the treatment | 20 |
| Micardis Plus before diagnosed date | 6 |
| no blood pressure recorded | 226 |
| unknown measuring date of BP | 118 |
| unable to evaluate | 104 |
| no recorded efficacy date | 34 |
| inconsistent BP measuring date | 4 |
Baseline Characteristics
| Description | |
|---|---|
| Hypertensive Patients With Micardis Plus for the First Time | In Post Marketing Surveillance (PMS), there are totally three figures. The number of enrolled patients: 6,901/ The number of patients for safety assessment: 6,606/ The number of patients for efficacy assessment: 6,120. |
| Hypertensive Patients With Micardis Plus for the First Time | |
|---|---|
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Number of Participants [units: participants] |
6606 |
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Age [units: years] Mean ± Standard Deviation |
59 ± 12 |
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Gender[1] [units: participants] |
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| Female | 3506 |
| Male | 3080 |
| [1] | In PMS, there are totally three figures. The number of enrolled patients: 6901/ The number of patients for safety assessment: 6606/ The number of patients for efficacy assessment: 6120. |
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Outcome Measures