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Telmisartan+HCTZ, Hypertension

This study is currently recruiting participants.
Verified by Boehringer Ingelheim Pharmaceuticals, July 2008

Sponsored by: Boehringer Ingelheim Pharmaceuticals
Information provided by: Boehringer Ingelheim Pharmaceuticals
ClinicalTrials.gov Identifier: NCT00659607
  Purpose

This PMS study aims to review the followings by investigating the actual practice of MicardisPlus Tablet on the market:

  1. Unexpected adverse drug reactions (especially, serious adverse events (SAEs))
  2. Frequency of incidence and its change in adverse events (AEs)
  3. Factors on the safety profile of the study drug
  4. Factors on the efficacy profile of the study drug

Condition Phase
Hypertension
Phase IV

MedlinePlus related topics:   High Blood Pressure   

ChemIDplus related topics:   Telmisartan    Telmisartan-Hydrochlorothiazide   

U.S. FDA Resources

Study Type:   Observational
Official Title:   PMS Study of MicardisPlus Tablet

Further study details as provided by Boehringer Ingelheim Pharmaceuticals:

Estimated Enrollment:   7000
Estimated Study Completion Date:   February 2009

  Eligibility
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

INCLUSION CRITERIA:

patients diagnosed as essential hypertension

EXCLUSION CRITERIA:

n/a

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00659607

Contacts
Contact: Boehringer Ingelheim Study Coordinator     clintriage@rdg.boehringer-ingelheim.com    

Locations
Korea, Republic of
Boehringer Ingelheim     Recruiting
      Busan, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Seoul, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Gyeonggido, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Gwangju, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Daegu, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Daejeon, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Chungnam, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Incheon, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Jeju, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Jeonnam, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Jeonbuk, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Ulsan, Korea, Republic of
Boehringer Ingelheim     Recruiting
      Gangwondo, Korea, Republic of

Sponsors and Collaborators
Boehringer Ingelheim Pharmaceuticals

Investigators
Study Chair:     Boehringer Ingelheim Study Coordinator     B.I. Korea Ltd.    
  More Information

Study ID Numbers:   502.475
First Received:   April 10, 2008
Last Updated:   July 25, 2008
ClinicalTrials.gov Identifier:   NCT00659607
Health Authority:   Korea, Republic of: KOREA Food and Drug Administration (KFDA)

Study placed in the following topic categories:
Vascular Diseases
Telmisartan
Hypertension

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on September 05, 2008




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