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Study to Evaluate Efficacy and Tolerability of Micardis®/Micardis® Plus in Patients With Hypertension

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Hypertension

Treatments

Drug: Micardis®
Drug: Micardis® Plus

Study type

Observational

Funder types

Industry

Identifiers

NCT02242357
502.427

Details and patient eligibility

About

Study to evaluate efficacy and tolerability of Micardis®/Micardis® Plus under usual daily-practice prescribing conditions in hypertensive patients

Enrollment

14,553 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males and females for whom a medical antihypertensive therapy is indicated
  • Age >= 18 years

Exclusion criteria

  • Age < 18 years

Trial design

14,553 participants in 1 patient group

Patients with hypertension
Treatment:
Drug: Micardis® Plus
Drug: Micardis®

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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