The Clinical Study to Evaluate the Efficacy and Safety of Fimasartan in Patients With Mild to Moderate Essential Hypertension
NCT01135212 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 290
Last updated 2012-08-24
Summary
The purpose of this clinical study is to evaluate and compare the efficacy and safety of Fimasartan (60mg / 120mg) with Candesartan(8mg) in patients with mild to moderate hypertension.
Conditions
Interventions
- DRUG
-
Fimasartan 60mg
Fimasartan 60mg for mild to moderate hypertension. Take a tablet(filled in Doubleblind capsule) every morning.
- DRUG
-
Fimasartan 120mg
Fimasartan 120mg for mild to moderate hypertension. Take a tablet(filled in Doubleblind capsule) every morning.
- DRUG
-
Candesartan cilexetil
Candesartan 8mg for mild to moderate hypertension. Take a tablet(filled in Doubleblind capsule) every morning.
Sponsors & Collaborators
-
Kyungpook National University Hospital
collaborator OTHER -
Gyeongsang National University Hospital
collaborator OTHER -
Keimyung University
collaborator OTHER -
Kosin University Gospel Hospital
collaborator OTHER -
Daegu Catholic University Medical Center
collaborator OTHER -
Dong-A medical center
collaborator UNKNOWN -
Pusan National University Yangsan Hospital
collaborator OTHER -
Yeungnam University Hospital
collaborator OTHER -
Ulsan University Hospital
collaborator OTHER -
Inje University
collaborator OTHER -
Pusan National University Hospital
collaborator OTHER -
Boryung Pharmaceutical Co., Ltd
lead INDUSTRY
Principal Investigators
-
ShungChull Chae, Doctor´s degree · KuyngPook National Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 19 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-04-30
- Primary Completion
- 2011-04-30
- Completion
- 2011-05-31
Countries
- South Korea
Study Locations
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