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

No results posted yet for this study

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01135212 on ClinicalTrials.gov