Working… Menu

Pharmaco-epidemiological Study Describing a Population of Hypertensive Patients Treated With a Fixed-dose Combination of Telmisartan and Hydrochlorothiazide

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT02248129
Recruitment Status : Completed
First Posted : September 25, 2014
Last Update Posted : September 25, 2014
Information provided by (Responsible Party):
Boehringer Ingelheim

Brief Summary:
Study to compare the level of blood pressure control in hypertensive, hypertensive diabetics and hypertensive with renal insufficiency (observed data) in the study population, with the objectives of the High Authority for Health recommendations (benchmark)

Condition or disease Intervention/treatment
Hypertension Drug: Telmisartan and hydrochlorothiazide

Layout table for study information
Study Type : Observational
Actual Enrollment : 4255 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Pharmaco-epidemiological Study Describing a Population of Hypertensive Patients Treated in General Practice With a Fixed-dose Combination of Telmisartan and Hydrochlorothiazide, the Level of Blood Pressure Control and the Modalities of Arterial Hypertension Management
Study Start Date : April 2006
Actual Primary Completion Date : December 2006

Resource links provided by the National Library of Medicine

Group/Cohort Intervention/treatment
Hypertensive patients Drug: Telmisartan and hydrochlorothiazide

Primary Outcome Measures :
  1. Percentage of patients with low blood pressure [ Time Frame: up to 4 weeks ]
    lower than 140/90 mmHg in the general population of hypertensive patients, hypertensive diabetics and hypertensive with renal insufficiency

Secondary Outcome Measures :
  1. Number of patients with adverse events [ Time Frame: up to 4 weeks ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Hypertensive patients treated in general practice

Inclusion Criteria:

  • Hypertensive patients already treated for at least 1 month with Telmisartan plus hydrochlorothiazide, consulting the physician consecutively for whatever reason

Exclusion Criteria:

  • NA

Additional Information:
Layout table for additonal information
Responsible Party: Boehringer Ingelheim Identifier: NCT02248129     History of Changes
Other Study ID Numbers: 502.508
First Posted: September 25, 2014    Key Record Dates
Last Update Posted: September 25, 2014
Last Verified: September 2014
Additional relevant MeSH terms:
Layout table for MeSH terms
Vascular Diseases
Cardiovascular Diseases
Antihypertensive Agents
Natriuretic Agents
Physiological Effects of Drugs
Sodium Chloride Symporter Inhibitors
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Angiotensin II Type 1 Receptor Blockers
Angiotensin Receptor Antagonists