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Post-Marketing Surveillance of Micardis® (Telmisartan) in Patients With Hypertension

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Hypertension

Treatments

Drug: Telmisartan

Study type

Observational

Funder types

Industry

Identifiers

NCT02242838
502.500

Details and patient eligibility

About

The primary objective of this survey is to prospectively investigate safety and efficacy in patients with hypertension treated with telmisartan in proper use in medical practice over a long period

Enrollment

6,336 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with hypertension

Exclusion criteria

Patients with the following conditions

  • Patients with a history of hypersensitivity of this product
  • Women in pregnancy (included the possibility of pregnancy)
  • Patients with severe biliary obstructive disorders or severe hepatic insufficiency

Trial design

6,336 participants in 1 patient group

Hypertensive patients
Treatment:
Drug: Telmisartan

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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