Trials / Completed
CompletedNCT01631227
Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressure in Essential Hypertension
A Prospective, Randomized Double-blind Parallel Group Study to Compare the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressure in Subjects With Mild to Moderate Essential Hypertension
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 665 (actual)
- Sponsor
- Abbott · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Aim of this study is to compare the blood pressure lowering effect of a new drug formulation of eprosartan. Eprosartan belongs to a class of blood pressure lowering agents used worldwide since years with proven efficacy. The new formulation is compared to the currently marketed eprosartan tablet. Equivalent efficacy in blood pressure lowering effects should be demonstrated.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Eprosartan | Eprosartan 450 mg |
| DRUG | Eprosartan Mesylate | Eprosartan mesylate 600 mg |
| DRUG | Placebo Eprosartan mesylate | Placebo Eprosartan mesylate |
| DRUG | Placebo Eprosartan | Placebo Eprosartan |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2013-04-01
- Completion
- 2013-04-01
- First posted
- 2012-06-29
- Last updated
- 2014-07-25
- Results posted
- 2014-05-26
Locations
38 sites across 3 countries: Germany, Russia, United Kingdom
Source: ClinicalTrials.gov record NCT01631227. Inclusion in this directory is not an endorsement.