Trials / Terminated
TerminatedNCT01766505
The Study to Evaluate Efficacy and Safety of Candesartan vs Losartan in Hypertension With Heart Failure (HONOR)
Randomized, Open-label, Phase 4 Study to Evaluate Efficacy and Safety of Candesartan and Losartan in the Patients With Hypertension and Heart Failure.
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Chong Kun Dang Pharmaceutical · Industry
- Sex
- All
- Age
- 19 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare efficacy and safety of candesartan and losartan in hypertension with heart failure.
Detailed description
This is a randomized, open-label, phase 4 study. wash out periods need at least 14 days if the patients take ARB or ACE inhibitor to control Blood pressure. Patients take Candemore or Cozzar once a day during 16 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Candemore tablet | Candemore tablet 8, 16, or 32mg/tab, per oral, a tablet once a day during 16 weeks. dosage is depends on the sitting blood pressure. |
| DRUG | Cozzar tablet | Cozzar tablet: 8mg, 16mg, 32mg/tablet, per oral, a tablet a day during 16 weeks dosage depends on sitting blood pressure |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2014-03-01
- Completion
- 2014-03-01
- First posted
- 2013-01-11
- Last updated
- 2014-03-14
Locations
9 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01766505. Inclusion in this directory is not an endorsement.