A Clinical Study to Evaluate Efficacy and Safety of Fimasartan/Hydrochlorothiazide Combination-therapy

NCT01258673 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 263

Last updated 2012-01-05

No results posted yet for this study

Summary

The purpose of this study is to evaluate the antihypertensive efficacy and safety of Fimasartan/Hydrochlorothiazide combination 60/12.5mg\~120/12.5mg in patients with essential hypertension who are not controlled by fimasartan 60mg.

Conditions

  • Essential Hypertension

Interventions

DRUG

Fimasartan/HCTZ combination

Fimasartan/HCTZ combination 60/12.5mg 120/12.5mg

DRUG

Fimasartan

Fimasartan 60mg, 120mg

Sponsors & Collaborators

  • Seoul National University Hospital

    collaborator OTHER
  • The Catholic University of Korea

    collaborator OTHER
  • Korea University Guro Hospital

    collaborator OTHER
  • DongGuk University

    collaborator OTHER
  • Seoul National University Bundang Hospital

    collaborator OTHER
  • Samsung Medical Center

    collaborator OTHER
  • Asan Medical Center

    collaborator OTHER
  • Gangnam Severance Hospital

    collaborator OTHER
  • Severance Hospital

    collaborator OTHER
  • Ajou University

    collaborator OTHER
  • Chonbuk National University Hospital

    collaborator OTHER
  • Cheil General Hospital and Women's Healthcare Center

    collaborator OTHER
  • Chonnam National University Hospital

    collaborator OTHER
  • Hanyang University

    collaborator OTHER
  • Yonsei University

    collaborator OTHER
  • Ilsan-Paik Hospital

    collaborator UNKNOWN
  • SMG-SNU Boramae Medical Center

    collaborator OTHER
  • Kyung Hee University Hospital

    collaborator OTHER
  • Boryung Pharmaceutical Co., Ltd

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2011-12-31

Countries

  • South Korea

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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 NCT01258673 on ClinicalTrials.gov