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Telmisartan 80mg+Hydrochlorothiazide (HCTZ) 25 mg in Hypertension: an Observational Study

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Hypertension

Study type

Observational

Funder types

Industry

Identifiers

NCT00909038
502.574

Details and patient eligibility

About

It is a national, retrospective , observational study in hypertensive patients treated for at least 8 weeks with the fixed dose combination of telmisartan 80 mg and hydrochlorothiazide 25 mg. The primary objective is to assess the control rate (systolic and diastolic blood pressure). Key secondary objectives are to assess the blood pressure reduction after at least 8 weeks of treatment, describe the population treated with this new fixed dose combination

Enrollment

2,411 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hypertensives
  • Treated for at least 8 weeks with the fixed dose combination of telmisartan 80 mg and hydrochlorothiazide 25 mg

Exclusion criteria

  • Treated with the combination less than 8 weeks

Trial contacts and locations

915

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Data sourced from clinicaltrials.gov

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