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Evaluation of Efficacy and Tolerability of Micardis® / MicardisPlus® Under Usual Daily-practice Prescribing in Patients With Hypertension

NCT ID: NCT02242383

Last Updated: 2014-09-17

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

13248 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-01-31

Brief Summary

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To evaluate efficacy and tolerability of Micardis® / MicardisPlus® under usual daily-practice prescribing conditions with a special emphasis on controlling morning blood pressure

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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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Essential hypertension

Telmisartan

Intervention Type DRUG

Telmisartan in combination with hydrochlorothiazide

Intervention Type DRUG

Interventions

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Telmisartan

Intervention Type DRUG

Telmisartan in combination with hydrochlorothiazide

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

\- Age ≥ 18 years, insufficiently treated hypertension

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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502.485

Identifier Type: -

Identifier Source: org_study_id

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