Pritor (Telmisartan , BAY68-9291)
DrugPrimary care hypertensive patients starting the therapy with Telmisartan
NCT Number: NCT00471003
The main purpose of this study is to asses the efficacy and safety of telmisartan, with the special attention on the influence of telmisartan on selected metabolic parameters of patients.
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Notify Me18 year and older
All sexes
Observational
Many Locations, Croatia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Primary care hypertensive patients starting the therapy with Telmisartan
Time frame: At the both of planned control visits. (Approx. interval between visits 3 months)
Time frame: At the both of planned control visits. (Approx. interval between visits 3 months)
Bayer
Industry
A Non-Interventional, Post-Marketing Surveillance Phase IV Study to Asses the Efficacy and Safety of Telmisartan, With the Special Attention on the Influence of Telmisartan on Selected Metabolic Parameters of Patients
Acronym: METABOLIC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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