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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 prim...
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Lead Sponsor
Boehringer Ingelheim
NCT02417740 · Cystic Fibrosis, Immunologic Deficiency Syndrome, and more
NCT07218029 · Pulmonary Arterial Hypertension
NCT07365332 · Pulmonary Arterial Hypertension
NCT06649110 · Healthy Volunteers, Pulmonary Arterial Hypertension
NCT06647511 · Gestational Hypertension
Boehringer Ingelheim Investigator site 1
Ablon-sur-Seine
Boehringer Ingelheim Investigator site 2
Achenheim
Boehringer Ingelheim Investigator site 3
Afa
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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