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Evaluation of Efficacy and Safety of the Dosage Adjustment of Aprovel® (Irbesartan) in Hypertensive Outpatients in Current Clinical Practice

Hypertension Clinical Trial

Official title:
Prospective, Multicentric, Randomized, Open, Comparative Phase IV Study Evaluating the Efficacy and Safety of the Dosage Adjustment of Aprovel® (Irbesartan) in Hypertensive Outpatients in Current Clinical Practice

Clinical Trial Summary

Primary:

- To evaluate the efficacy of two regimens of irbesartan in patients responding but not normalized at 6 weeks of treatment (schema N°1: maintenance 150 mg/day, schema n°2: 300 mg/day for 6 more weeks)

Secondary:

- To evaluate the percentage of patients with DBP < 90 mmHg at 6 and 12 weeks

- To evaluate the percentage of patients with SBP < 140 mmHg at 6 and 12 weeks

- To evaluate rate of adverse events during the study

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00564187
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date February 2003
Completion date December 2004
View Details
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