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The Real-Life Efficacy and Safety of Telmisartan in Patients With Arterial Hypertension (METABOLIC)

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Bayer

Status

Completed

Conditions

Hypertension

Treatments

Drug: Pritor (Telmisartan , BAY68-9291)

Study type

Observational

Funder types

Industry

Identifiers

NCT00471003
13929 - KL0601SI
14326 - KL0601HR
KL0601PL
12804 - KL0601SK
12729

Details and patient eligibility

About

The main purpose of this study is to asses the efficacy and safety of telmisartan, with the special attention on the influence of telmisartan on selected metabolic parameters of patients.

Enrollment

5,448 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age over 18
  • Untreated or ineffectively treated arterial hypertension

Exclusion criteria

  • Cholestatic disorders and severe hepatic failure
  • Allergy to telmisartan
  • Pregnancy and lactation period

Trial design

5,448 participants in 1 patient group

Arm 1
Treatment:
Drug: Pritor (Telmisartan , BAY68-9291)

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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