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Post-Marketing Surveillance Study of Micardis® Plus in Patients With Hypertension

NCT ID: NCT02238275

Last Updated: 2014-09-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

8135 participants

Study Classification

OBSERVATIONAL

Study Start Date

2002-06-30

Brief Summary

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Study to evaluate efficacy and tolerability of Micardis® plus under usual daily-practice prescribing-conditions

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Detailed Description

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Conditions

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Hypertension

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with hypertension

Micardis® plus

Intervention Type DRUG

Interventions

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Micardis® plus

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Adult (Age \>= 18 years) males and females for whom a medical antihypertensive therapy is indicated

Exclusion Criteria

* Age \< 18 years
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Boehringer Ingelheim

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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502.390

Identifier Type: -

Identifier Source: org_study_id

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