ClinicalTrials.gg
CompletedNCT00539487Updated Nov 8, 2013

Observational Non-interventional Study (Anwendungsbeobachtung) With Telmisartan in High-risk Hypertensives

An observational study in Hypertension and Obesity, sponsored by Boehringer Ingelheim. Completed at 2,389 sites in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-11-08.

Sponsored by Boehringer Ingelheim · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
5,827
Ages
18 Years and older
Sex
All
01

Study summary

This observational non-interventional study will assess (under conditions of clinical practice in daily routine) the antihypertensive efficacy of telmisartan treatment with or without active promotion of lifestyle changes in hypertensive patients at high cardiovascular risk

Read the detailed description

Study Design:

02

Conditions studied

  • Hypertension
  • Obesity
03

In context

Hypertension

6,834 studies on the registry are indexed under Hypertension; 971 are open to participants now.

This study's enrollment of 5,827 is above the median of 210 across 1,392 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Boehringer Ingelheim is the lead sponsor of 2,297 studies on the registry; 56 are open to participants now.

Of its 166 completed or terminated interventional studies of FDA-regulated products, 121 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

hypertensive patients

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

patients with essential hypertension aged >/= 18 years with one of the following risk factors: history of coronary artery disease or stroke/TIA or peripheral artery disease or diabetes mellitus.

Exclusion criteria

Exclusion Criteria:

according to SPC

05

Study design

Time perspective
Prospective
Enrollment
5,827 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Blood pressure reduction

    Time frame: 4 month

Secondary outcomes

  1. Change in metabolic parameters Safety

07

Study locations

2,389 sites
  • Boehringer Ingelheim Investigational Site 1
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 2
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 3
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 4
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 5
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 6
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 7
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site 8
    Aachen, Germany
  • Boehringer Ingelheim Investigational Site
    Aalen, Germany
  • Boehringer Ingelheim Investigational Site
    Aarbergen, Germany
  • Boehringer Ingelheim Investigational Site
    Abstatt, Germany
  • Boehringer Ingelheim Investigational Site
    Achern, Germany
  • Boehringer Ingelheim Investigational Site 1
    Adendorf, Germany
  • Boehringer Ingelheim Investigational Site 2
    Adendorf, Germany
  • Boehringer Ingelheim Investigational Site 3
    Adendorf, Germany
  • Boehringer Ingelheim Investigational Site
    Aham, Germany
  • Boehringer Ingelheim Investigational Site 1
    Ahaus, Germany
  • Boehringer Ingelheim Investigational Site 2
    Ahaus, Germany
  • Boehringer Ingelheim Investigational Site
    Ahlen, Germany
  • Boehringer Ingelheim Investigational Site
    Ahorn, Germany
  • Boehringer Ingelheim Investigational Site
    Ahorntal, Germany
  • Boehringer Ingelheim Investigational Site
    Ahrensbök, Germany
  • Boehringer Ingelheim Investigational Site
    Ahrensburg, Germany
  • Boehringer Ingelheim Investigational Site
    Ahrensfelde, Germany
  • Boehringer Ingelheim Investigational Site
    Aichach, Germany
  • Boehringer Ingelheim Investigational Site
    Aichtal, Germany
  • Boehringer Ingelheim Investigational Site
    Ainring, Germany
  • Boehringer Ingelheim Investigational Site
    Albbruck, Germany
  • Boehringer Ingelheim Investigational Site 1
    Albstadt, Germany
  • Boehringer Ingelheim Investigational Site 2
    Albstadt, Germany
  • Boehringer Ingelheim Investigational Site 3
    Albstadt, Germany
  • Boehringer Ingelheim Investigational Site 4
    Albstadt, Germany
  • Boehringer Ingelheim Investigational Site
    Aldenhoven, Germany
  • Boehringer Ingelheim Investigational Site
    Alfeld, Germany
  • Boehringer Ingelheim Investigational Site
    Algermissen, Germany
  • Boehringer Ingelheim Investigational Site
    Allendorf, Germany
  • Boehringer Ingelheim Investigational Site
    Allmendingen, Germany
  • Boehringer Ingelheim Investigational Site 1
    Alpen, Germany
  • Boehringer Ingelheim Investigational Site 2
    Alpen, Germany
  • Boehringer Ingelheim Investigational Site
    Alsdorf, Germany
  • Boehringer Ingelheim Investigational Site
    Altena, Germany
  • Boehringer Ingelheim Investigational Site 1
    Altenburg, Germany
  • Boehringer Ingelheim Investigational Site 2
    Altenburg, Germany
  • Boehringer Ingelheim Investigational Site 1
    Altenholz, Germany
  • Boehringer Ingelheim Investigational Site 2
    Altenholz, Germany
  • Boehringer Ingelheim Investigational Site 3
    Altenholz, Germany
  • Boehringer Ingelheim Investigational Site 1
    Altenstadt, Germany
  • Boehringer Ingelheim Investigational Site 2
    Altenstadt, Germany
  • Boehringer Ingelheim Investigational Site
    Altensteig, Germany
  • Boehringer Ingelheim Investigational Site
    Altlußheim, Germany
  • Boehringer Ingelheim Investigational Site
    Altmittweida, Germany
  • Boehringer Ingelheim Investigational Site
    Altötting, Germany
  • Boehringer Ingelheim Investigational Site
    Altrip, Germany
  • Boehringer Ingelheim Investigational Site
    Alzenau in Unterfranken, Germany
  • Boehringer Ingelheim Investigational Site
    Amberg, Germany
  • Boehringer Ingelheim Investigational Site
    Ammerbuch, Germany
  • Boehringer Ingelheim Investigational Site
    Anklam, Germany
  • Boehringer Ingelheim Investigational Site
    Ansbach, Germany
  • Boehringer Ingelheim Investigational Site
    Apelern, Germany
  • Boehringer Ingelheim Investigational Site 1
    Apolda, Germany
  • Boehringer Ingelheim Investigational Site 2
    Apolda, Germany
  • Boehringer Ingelheim Investigational Site
    Appenweier, Germany
  • Boehringer Ingelheim Investigational Site
    Arenshausen, Germany
  • Boehringer Ingelheim Investigational Site
    Artern, Germany
  • Boehringer Ingelheim Investigational Site 1
    Arzberg, Germany
  • Boehringer Ingelheim Investigational Site 2
    Arzberg, Germany
  • Boehringer Ingelheim Investigational Site
    Aschaffenburg, Germany
  • Boehringer Ingelheim Investigational Site 1
    Aschersleben, Germany
  • Boehringer Ingelheim Investigational Site 2
    Aschersleben, Germany
  • Boehringer Ingelheim Investigational Site
    Aspach, Germany
  • Boehringer Ingelheim Investigational Site
    Attendorn, Germany
  • Boehringer Ingelheim Investigational Site
    Attenkirchen, Germany
  • Boehringer Ingelheim Investigational Site
    Auerbach, Germany
  • Boehringer Ingelheim Investigational Site 1
    Augsburg, Germany
  • Boehringer Ingelheim Investigational Site 2
    Augsburg, Germany
  • Boehringer Ingelheim Investigational Site 3
    Augsburg, Germany
  • Boehringer Ingelheim Investigational Site 4
    Augsburg, Germany
  • Boehringer Ingelheim Investigational Site 5
    Augsburg, Germany
  • Boehringer Ingelheim Investigational Site
    Auw, Germany
  • Boehringer Ingelheim Investigational Site 1
    Aßlar, Germany
  • Boehringer Ingelheim Investigational Site 2
    Aßlar, Germany
  • Boehringer Ingelheim Investigational Site
    Baar-Ebenhausen, Germany
  • Boehringer Ingelheim Investigational Site
    Babenhausen, Germany
  • Boehringer Ingelheim Investigational Site 1
    Backnang, Germany
  • Boehringer Ingelheim Investigational Site 2
    Backnang, Germany
  • Boehringer Ingelheim Investigational Site 3
    Backnang, Germany
  • Boehringer Ingelheim Investigational Site 1
    Bad Bentheim, Germany
  • Boehringer Ingelheim Investigational Site 2
    Bad Bentheim, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Berka, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Bevensen, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Blankenburg, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Doberan, Germany
  • Boehringer Ingelheim Investigational Site 1
    Bad Düben, Germany
  • Boehringer Ingelheim Investigational Site 2
    Bad Düben, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Dürrenberg, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Dürrheim, Germany
  • Boehringer Ingelheim Investigational Site 1
    Bad Elster, Germany
  • Boehringer Ingelheim Investigational Site 2
    Bad Elster, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Ems, Germany
  • Boehringer Ingelheim Investigational Site
    Bad Essen, Germany

Showing the first 100 of 2,389 sites.

08

References and documents

Related links

09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2007 and a primary completion of Nov 2007. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 25, 2007
First posted
Oct 4, 2007
Start
Jan 2007
Primary completionActual
Nov 2007
Last update
Nov 8, 2013
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 8, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00539487
First posted
Oct 4, 2007
Start date
Jan 2007
Primary completion
Nov 2007
Last update
Nov 8, 2013

Study contacts

Boehringer Ingelheim
study chair · Boehringer Ingelheim
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2013. You cannot join it, but the record below documents what was studied.

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