Trials / Completed
CompletedNCT01918332
Efficacy and Safety of Valsartan 160mg and Rosuvastatin 20mg in Patients With Hypertension and Hyperlipidemia
A Multicenter, Randomized, Factorial, Double-blinded, Double-dummy Phase Ⅲ Trial to Evaluate the Efficacy and Safety of the Coadministration of Valsartan 160mg and Rosuvastatin 20mg in Comparison to Each Component Administered Alone in Patients With Hypertension and Hyperlipidemia
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 168 (actual)
- Sponsor
- LG Life Sciences · Industry
- Sex
- All
- Age
- 20 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to evaluate the efficacy and safety of the coadministration of valsartan (Diovan®) 160mg and rosuvastatin (Crestor®) 20mg in comparison to each component administered alone in patients with hypertension and hyperlipidemia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Valsartan 160mg | |
| DRUG | Rosuvastatin 20mg | |
| DRUG | Valsartan 160mg placebo | |
| DRUG | Rosuvastatin 20mg placebo |
Timeline
- Start date
- 2012-04-01
- Primary completion
- 2013-03-01
- Completion
- 2013-03-01
- First posted
- 2013-08-07
- Last updated
- 2014-12-15
- Results posted
- 2014-12-15
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01918332. Inclusion in this directory is not an endorsement.